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Sample records for acrylic acid

  1. Acrylic Acid and Esters Will Be Oversupply

    Zheng Chengwang

    2007-01-01

    @@ Drastic capacity growth The production capacity of acrylic acid in China has grown drastically in recent years. With the completion of the 80 thousand t/a acrylic acid and 130 thous and t/a acrylic ester project in Shenyang Paraffin Chemical Industrial Co., Ltd., (CCR2006,No. 31) the capacity of acrylic acid in China has reached 882 thousand t/a.

  2. 21 CFR 573.120 - Acrylamide-acrylic acid resin.

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Acrylamide-acrylic acid resin. 573.120 Section 573... Food Additive Listing § 573.120 Acrylamide-acrylic acid resin. Acrylamide-acrylic acid resin... acrylamide with partial hydrolysis, or by copolymerization of acrylamide and acrylic acid with the...

  3. Radiochemical coupling of acrylic acid to polyvinylchloride

    Acrylic acid was coupled radiochemically to the surface of polyvinylchloride (PVC) foils. A 500 keV electron generator served as radiation source. After neutralization with ammonia, the surface of the PVC foils got hydrophilic properties. Their capacity of water uptake increased from 0,04 mg/cm2 to about 0,5 mg/cm2 and the condensation of water takes place in form of a clear transparent film and not in form of light scattering droplets. 6 refs., 20 figs., 8 tabs

  4. Radiation-induced graft copolymerization of methyl acrylate and acrylic acid onto rubber wood fiber

    Graft copolymerization of methyl acrylate and acrylic acid monomers onto rubber wood fiber (RWF) was carried out by simultaneous radiation-induced technique. The parameters affecting the grafting reaction were investigated and the optimum conditions for both monomers obtained are as follows: impregnation time = 16 hours, total dose = 30 kGy, methanol : water ratio, 3:1, monomers concentration = 40 v/v % and sulphuric acid concentration = 0.1 mol/L. Fourier Transform Infrared (FTIR), thermogravimetry analysis (TGA), and scanning electron microscope (SEM) analyses used to characterize graft copolymers. The structural investigation by x-ray diffraction (XRD) shows the degree of crystallinity of rubber wood fiber decreased with the incorporation of poly(methyl acrylate) and poly(acrylic acid) grafts. (Author)

  5. Radiation induced grafting of acrylic acid onto extruded polystyrene surface

    Polystyrene materials with good solubility in liquid scintillation cocktails are used to wipe off different types of surfaces in order to determine the tritium removable contamination with the help of a liquid scintillation counter. This paper analyses hydrophilic surface modifications by radiation induced grafting of acrylic groups onto extruded polystyrene plates. Two grafting methods were used: (a) exposure of extruded polystyrene plates, immersed in aqueous acrylic acid solution, to a gamma radiation of a Co-60 source, and (b) exposure of extruded polystyrene plates to a Co-60 source, followed by the immersion of extruded polystyrene plates in aqueous acrylic acid solution. The grafting of acrylic was proved by IR spectrometry and by radiometric methods using acrylic acid labelled with tritium. - Highlights: ► Polystyrene (PS) is used to determine the removable surface contamination (RSC). ► RSC factor may be increased by PS surface modification. ► PS surface was modified by acrylic acid grafting using γ radiation 60Co source. ► Acrylic fragments insertion was determined by IR, and radiometric. ► Grafted PS discs increase RSC factor in the case of tritium contamination.

  6. Rare linking hydrogels based on acrylic acid and carbohydrate esters

    U. Akhmedov

    2012-09-01

    Full Text Available The process of copolymerization of acrylic acid and esters poliallil sucrose; pentaerythritol and sorbitol, some of its laws are identified. The kinetic regularities of copolymerization and the optimum conditions of synthesis was established.

  7. Antimicrobial activity of poly(acrylic acid) block copolymers

    Gratzl, Günther, E-mail: guenther.gratzl@jku.at [Johannes Kepler University Linz, Institute for Chemical Technology of Organic Materials, Altenberger Str. 69, 4040 Linz (Austria); Paulik, Christian [Johannes Kepler University Linz, Institute for Chemical Technology of Organic Materials, Altenberger Str. 69, 4040 Linz (Austria); Hild, Sabine [Johannes Kepler University Linz, Institute of Polymer Science, Altenberger Str. 69, 4040 Linz (Austria); Guggenbichler, Josef P.; Lackner, Maximilian [AMiSTec GmbH and Co. KG, Leitweg 13, 6345 Kössen, Tirol (Austria)

    2014-05-01

    The increasing number of antibiotic-resistant bacterial strains has developed into a major health problem. In particular, biofilms are the main reason for hospital-acquired infections and diseases. Once formed, biofilms are difficult to remove as they have specific defense mechanisms against antimicrobial agents. Antimicrobial surfaces must therefore kill or repel bacteria before they can settle to form a biofilm. In this study, we describe that poly(acrylic acid) (PAA) containing diblock copolymers can kill bacteria and prevent from biofilm formation. The PAA diblock copolymers with poly(styrene) and poly(methyl methacrylate) were synthesized via anionic polymerization of tert-butyl acrylate with styrene or methyl methacrylate and subsequent acid-catalyzed hydrolysis of the tert-butyl ester. The copolymers were characterized via nuclear magnetic resonance spectroscopy (NMR), size-exclusion chromatography (SEC), Fourier transform infrared spectroscopy (FTIR), elemental analysis, and acid–base titrations. Copolymer films with a variety of acrylic acid contents were produced by solvent casting, characterized by atomic force microscopy (AFM) and tested for their antimicrobial activity against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. The antimicrobial activity of the acidic diblock copolymers increased with increasing acrylic acid content, independent of the copolymer-partner, the chain length and the nanostructure. - Highlights: • Acrylic acid diblock copolymers are antimicrobially active. • The antimicrobial activity depends on the acrylic acid content in the copolymer. • No salts, metals or other antimicrobial agents are needed.

  8. Antimicrobial activity of poly(acrylic acid) block copolymers

    The increasing number of antibiotic-resistant bacterial strains has developed into a major health problem. In particular, biofilms are the main reason for hospital-acquired infections and diseases. Once formed, biofilms are difficult to remove as they have specific defense mechanisms against antimicrobial agents. Antimicrobial surfaces must therefore kill or repel bacteria before they can settle to form a biofilm. In this study, we describe that poly(acrylic acid) (PAA) containing diblock copolymers can kill bacteria and prevent from biofilm formation. The PAA diblock copolymers with poly(styrene) and poly(methyl methacrylate) were synthesized via anionic polymerization of tert-butyl acrylate with styrene or methyl methacrylate and subsequent acid-catalyzed hydrolysis of the tert-butyl ester. The copolymers were characterized via nuclear magnetic resonance spectroscopy (NMR), size-exclusion chromatography (SEC), Fourier transform infrared spectroscopy (FTIR), elemental analysis, and acid–base titrations. Copolymer films with a variety of acrylic acid contents were produced by solvent casting, characterized by atomic force microscopy (AFM) and tested for their antimicrobial activity against Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. The antimicrobial activity of the acidic diblock copolymers increased with increasing acrylic acid content, independent of the copolymer-partner, the chain length and the nanostructure. - Highlights: • Acrylic acid diblock copolymers are antimicrobially active. • The antimicrobial activity depends on the acrylic acid content in the copolymer. • No salts, metals or other antimicrobial agents are needed

  9. Textile dyestuff adsorption by polysaccharide-g-acrylic acid

    Aimed of this study to determine the ability of polysacharide of banana peel as an adsorbent of textile dyes (Maxilon Yellow) before and after the grafting process. The grafting copolymerization process was done by using acrylic acid as monomer, then irradiated by gamma rays as initiator. Parameters observed were adsorption ability of dye, soaking time with KOH, acrylic acid concentration, irradiation dose and resistance to acids. The results showed the optimum absorption obtained at the time of KOH immersion for 3 hours, the concentration of acrylic acid by 20% and the irradiation dose of 30 kGy. Adsorption percentage of polysacharide to Maxilon Yellow after grafting increased by 18,48% compared to before grafting. Resistance to the acid test increased significantly. The results of this study are expected to overcome the problems of waste dyes in the textile industry. (author)

  10. COMPLEX OXIDE CATALYSTS OF ACRYLIC ACID OBTAINING BY ALDOL CONDENSATION METHOD

    Nebesnyi, R.

    2015-01-01

    The present work is dedicated to solving the problem of diversification of the raw materials base for acrylate monomers obtaining,  first of all acrylic acid. Acrylic acid and its derivatives are bulk products of organic synthesis with a wide range of applications. The main industrial method of acrylic acid production is  propylene oxidation. But this method has instable economic indicators as propylene is petroleum origin raw material.It is possible to expand the resource base of acrylic aci...

  11. Decarboxylation-based traceless linking with aroyl acrylic acids

    Nielsen, John

    1998-01-01

    beta-Keto carboxylic acids are known to decarboxylate readily. In our pursuit to synthesize beta-indolinyl propiophenones, we have exploited this chemistry as a mean of establishing a traceless handle. 2-Aroyl acrylic acids have been esterified to a trityl resin, after which Michael-type addition...

  12. 21 CFR 176.110 - Acrylamide-acrylic acid resins.

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Acrylamide-acrylic acid resins. 176.110 Section 176.110 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS Substances for Use Only as Components of Paper...

  13. Use of Acrylic Acid Sodium Acrylate Polymer to Maintain Cocoa Seed Viability

    Pudji Rahardjo

    2010-08-01

    Full Text Available The main problem of cocoa seed storage is moisture content of the seeds because cocoa seeds will germinate if cocoa seeds moisture content is high. The objective of this research is to maintain the cocoa seeds viability in storage using acrylic acid sodium acrylate polymer (AASAP. The function of AASAP is to absorb humidity in storage due to their ability to retain water and to prevent water loss. The experiment was conducted in a laboratory of Indonesian Coffee and Cocoa Research Institute and in Kaliwining Experimental Garden. This experiment was arranged by factorial randomized complete design, in wich AASAP dosages 0%; 0.1% (0.1 g/100 seeds; 0.2% (0.2 g/100 seeds, 0.3% (0.3 g/100 seeds, 0,4% (0,4g/100 seeds, combined with seeds storage period 1, 2, 3 and 4 weeks. The experiment used 3 replications and each repli cation used 100 seeds. Parameter of observation consisted of percentage of seeds germinated in storage, percentage of seeds infected by fungi in storage, seeds moisture content, percentage of seeds germination after storage, and early growth of cocoa seedlings. The results of the experiment showed that AASAP application with some dosages cocoa seeds storage cause to germinate in storage during 2 weeks. AASAP application with some dosages in cocoa seeds storage for 2 weeks would not result in infection by fungi and did not significantly affect seed germination after storage for 1, 2 and 4 weeks, and percentage of germination of cocoa seed after storage for 3 weeks decreased with increase dosage of AASAP. Higher dosage of AASAP would reduce early growth of cocoa seedling. Key words : Theobroma cacao, seed, acrylic acid sodium acrylate, seed storage, viabilty.

  14. Radioinduced grafting of acrylic acid on expanded polystyrene matrices

    The unfixed surface radioactive contamination for low energy β radionuclides (3H and 14C) is determined by wiping the checked surfaces with sponge of absorbent materials. The activity built up by this sponge is measured by a liquid scintillator spectrometer. In this work, a method of obtaining sponges of expanded polystyrene with hydrophobic surface by radioinduced grafting of the acrylic acid is presented. These sponges have diameters of 28 mm, thicknesses of 1.5 - 2 mm and density of 22 mg/cm3. The samples were immersed in a grafting solution with the following composition: acrylic acid 30%, Cu SO4 1%; water 69% which were deeply impregnated in repeated operations under vacuum and pressure conditions, respectively. Finally, the samples were exposed to γ radiation emitted by a 60Co source (IETI 10 000 - IFIN-HH). The dose rates were 0.3, 0.5 and 1 Mrad/h. The range of the absorbed doses was 1 - 25 Mrad. The yields of radiochemical grafting have been determined by gravimetric, spectrophotometric and radiometric methods. The grafting agent used was 3H labelled acrylic acid. The solvation capacity and the quenching characteristics of the grafted sponges in liquid scintillators, as well as the sampling yields have been analyzed as function of irradiation procedure and the percentage of grafted acrylic fragments. The superficial grafting of the acrylic acid has been carried out by the mentioned technique, leading to the increase of the wiping efficiency of the unfixed surface contaminating activity, without changes of polymer solubility in liquid scintillators and without the perturbation of the radioactivity detection process. (authors)

  15. Acrylic acid obtaining from methanol and acetic acid in the presence of complex oxide catalysts

    Небесний, Роман Володимирович; Піх, Зорян Григорович; Шпирка, Ірина Іванівна; Івасів, Володимир Васильович; Небесна, Юлія Віталіївна; Фуч, Уляна Василівна

    2015-01-01

    The purpose of this work is to research process of single-stage acrylic acid obtaining from methanol and acetic acid, namely: to develop effective catalysts for the process of methanol oxidation to formaldehyde with its further aldol condensation with acetic acid to acrylic acid, and to determine optimum conditions for the process. Complex oxide catalysts consisting of oxides of boron, phosphorus, tungsten and vanadium supported on the silica gel have been investigated. The effect of vanadium...

  16. Scientific Opinion on the safety evaluation of the active substance, acrylic acid, sodium salt, co-polymer with acrylic acid, methyl ester, methacrylic acid, 2 hydroxypropylester, and acrylic acid cross-linked for use in active food contact materials

    EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF

    2013-04-01

    Full Text Available This scientific opinion of the EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids deals with the safety evaluation of the acrylic acid, sodium salt, co-polymer with acrylic acid, methyl ester, methacrylic acid, 2 hydroxypropylester, and acrylic acid cross-linked (CAS No. 117675-55-5, FCM Substance No 1022, to be used as liquid absorber in the form of fibres in absorbent pads for the packaging of fresh or frozen meat, poultry, and fish as well as fresh fruits and vegetables. The Panel considered that migration is not expected when the absorption capacity of the pads is not exceeded. Therefore no exposure from the consumption of the packed food is expected. The Panel also considered that none of these starting substances and the cross-linked polymer gives rise to concern for genotoxicity. Therefore the CEF Panel concluded that the use of the substance acrylic acid, sodium salt, co-polymer with acrylic acid, methyl ester, methacrylic acid, 2 hydroxypropylester, and acrylic acid cross-linked does not raise a safety concern when used as fibres in absorber pads for the packaging of fresh or frozen meat, poultry, fish, fruits and vegetables under conditions under which the absorption capacity of the pads is not exceeded and mechanical release of the fibres from the pads is excluded.

  17. A New Process for Acrylic Acid Synthesis by Fermentative Process

    Lunelli, B. H.; Duarte, E. R.; de Toledo, E. C. Vasco; Wolf Maciel, M. R.; Maciel Filho, R.

    With the synthesis of chemical products through biotechnological processes, it is possible to discover and to explore innumerable routes that can be used to obtain products of high addes value. Each route may have particular advantages in obtaining a desired product, compared with others, especially in terms of yield, productivity, easiness to separate the product, economy, and environmental impact. The purpose of this work is the development of a deterministic model for the biochemical synthesis of acrylic acid in order to explore an alternative process. The model is built-up with the tubular reactor equations together with the kinetic representation based on the structured model. The proposed process makes possible to obtain acrylic acid continuously from the sugar cane fermentation.

  18. Surface cross-linked humic acid - polysodium acrylate superabsorbent

    Chu, M.; Zhu, S.; Li, H.; Huang, Z.; Zhang, X. [China University of Mining and Technology, Beijing (China)

    2005-03-01

    A novel composite super-absorbent of humic acid-polysodium acrylate was invented by surface cross-linking reaction of lignite humic acid and poly. Humic acid was abstracted from leonardite and poly was synthesized by solution polymerization. Water absorbing mechanism of composite superabsorbent was explored based on FTIR and SEM. The effect of surface cross-linking reaction conditions, such as the ratio of methanol to water, cross-linking agent concentration, and the amount of humic acid on water absorbing were investigated. Experiments show that the water absorbency of superabsorbent can be greatly improved by humic acid. When the mass fraction of humic acid is 10%, the ratio of cross-linking agent to PSA is 0.2%, and the ratio of methanol to water is 1.8, the water absorbency is the best: 750 g/g for deionied water and 260 g/g for running. water. 9 refs., 5 figs., 1 tab.

  19. Conformational Transition of Poly (Acrylic Acid) Detected by Microcantilever Sensing

    LI Kai; LIU Hong; ZHANG Qing-Chuan; XUE Chang-Guo; WU Xiao-Ping

    2007-01-01

    Poly (acrylic acid) (PAA) chains are grafted on one side of a microcantilever by the self-assembled method and the deflections of the microcantilever are detected as a function of medium pH from 3 to 11. It is found that when the pH varies, the microcantilever deflects because of the changing surface stress. By analysing the electrostatic repulsive effect, the surface stress change is related to the conformation transition of PAA from a collapse state to a swelling state. This method offers the interaction information among the polymer chains during the conformational transition and affords an alternative way to study conformational change of polymers.

  20. Swelling Behaviors of Polyaniline-Poly(Acrylic Acid) Hydrogels

    ZHANG You-wei; ZHAO Jiong-xin; LI Xiao-feng; TAO Yong; WU Cheng-xun

    2005-01-01

    Using poly(acrylic acid) (PAA) aqueous solution, NaOH aqueous solution, aniline(An) and ammonim persulfate(APS), PAn-PAA hydrogels with a semi-interpenetrating structure connected by physical interlocks, chemical ion bonds and hydrogen bonds wcre prepared. The swelling properties of the hydrogels in solutions of different pH values(adjusted by adding NaOH or HCl) were studied. All the hydrogels prepared have similar swelling curves (the curves of equilibrium swelling ratio vs. pH value) and reach their maximum swelling at pH of 8 - 10. The maximum swelling ratio of the hydrogels is dependent on composition, including molecular weight of PAA, polymer content of the hydrogel,and molar ratios of AA to An, APS to An, and NaOH to AA.And the compositional dependence of the swelling capacity of PAn-PAA hydrogels was also studied.

  1. New initiation system for polymerization of acryl acid

    LI Hai-pu; ZHONG Hong; CHEN Qi-yuan; YIN Zhou-lan

    2005-01-01

    The redox initiation system for polyacrylate sodium of high molecular mass was designed and its effect with varying component dosage on the degree of polymerization was investigated. The results show that the proper type and amount of inorganic salt, as well as amine initiator, are conductive to the increase of degree of polymerization. The fine ingredient of the initiation system is as follows:the dosages of amine, persulphate and inorganic salt are 0.75%, 0.10% and 1.00% by mass based on acryl acid respectively, the molar ratio of sulphite to the persulphate is 1:1. Under such conditions the degree of polyacrylate can reach 7.43×107 with a acceptable polymerization time for industrial production.

  2. Polymerisation by acrylamide and acrylic acid inverse suspension

    Sergio Alejandro LLoreda Blanco

    2010-04-01

    Full Text Available This work describes polymerisation by inverse suspension of acrylamide monomers and acrylic acid for forming homopolymers or copolymers This type of polymersitaion's advantages are described and reasons given for why it should be studied. The article stresses the importance of these types of monomer for obtaining materials presenting great affinity for water, such as super-absorbents and controlled liberation mechanism. Important aspects are presented such as type of initiation, monomer composition and continuous phase composition; parameters are described offering an important basis for formulating a system leading to successfully obtaining the desired materials' most relevant characteristics such as particle distribution and size polymerisation kinetics, conversion and water absorption capacity respecting the system's modifiable parameters. The foregoing is important since the product can be modified, bestowing propierties on it which are suitable for its use.

  3. Study on preirradiation grafting of acrylic acid to cotton cellulose

    Grafting copolymerization of acrylic acid to cotton cellulose by using pre-irradiating method was investigated. At lower concentration of monomer (10%) the relationship between grafting yield and total dose, dose rate, reaction time and reaction temperature was measured. It was found that in the temperature range of 294 K to 323 K the grafting yield decreased with increasing of grafting reaction temperature. The grafting yields as a function of above reaction conditions were given by the expression Gr% = 5.9 x 10-10De20.27/RT(1-e-0.313te-6.87/RT), where R 8.314 x 10-3kj·K-1·mol-1, D = irradiation dose, T = reaction temperature, and t = reaction time

  4. Copolymerization of Indene with Acrylic Acid, Itaconic Acid and Acrylonitrile: Characterization and Reactivity Ratios

    Random copolymers of indene (In) with acrylic acid (AA), itaconic acid (IA) and acrylonitrile (AN) were synthesized by free radical polymerization in dioxane in the presence of azobisisobutyronitrile as an initiator at 60 degree C. The homopolymer of indene and acrylonitrile was prepared using K2MnO4 and sulphuric acid as an initiator, while acrylic acid and itaconic acid were prepared using K2S2O8 solution. The reactivity ratios of the monomers were calculated by different methods. X-ray diffraction as well as thermal analyses were studied. The latter was studied via thermogravimetric analysis and differential thermal analysis. The complexation with metal ions such as Cu+2 and Fe+2 was investigated. The copolymerization and the complexation processes were confirmed by FTIR spectroscopy. Also the activation energy of the prepared copolymers was determined

  5. Synthesis of poly(N-isopropylacrylamide-co-acrylic acid) model compounds for filtration experiments

    Hinge, Mogens; Christensen, Morten Lykkegaard; Scales, Peter;

    2005-01-01

    microgels. Capillary rheometry indicates that the blocks of poly(acrylic acid) are placed on the surface of the microgels. The combination of these three results reveal that the microgels have a core mainly consisting of poly(N-isopropylacrylamide) and a diffuse/cloudy surface consisting mainly of poly(acrylic...

  6. Blends of dissolved cellulose with acrylic acid copolymers or microfibrillated cellulose

    Saarikoski, Eve

    2015-01-01

    The aim of the thesis was to develop dissolved cellulose (dissolved in NaOH/ZnO) based blends with acrylic acid copolymers (poly(ethylene-co-acrylic acid) (PE-co-AA) or poly(acrylamide-co-acrylic acid) (PAA-co-AA)) or microfibrillated cellulose (MFC) in the way they could be used in injection molding or for film/coating applications. This thesis summarizes the research reported in five publications supported by some unpublished results. Rheological studies done in the contexts of this work...

  7. Catalytic routes towards acrylic acid, adipic acid and epsilon-caprolactam starting from biorenewables

    Beerthuis, R.; Rothenberg, G.; Shiju, N.R.

    2015-01-01

    The majority of bulk chemicals are derived from crude oil, but the move to biorenewable resources is gaining both societal and commercial interest. Reviewing this transition, we first summarise the types of today's biomass sources and their economical relevance. Then, we assess the biobased productions of three important bulk chemicals: acrylic acid, adipic acid and epsilon-caprolactam. These are the key monomers for high-end polymers (polyacrylates, nylon 6.6 and nylon 6, respectively) and a...

  8. Poly (ethylene oxide)-block-poly (n-butyl acrylate)-blockpoly (acrylic acid) triblock terpolymers with highly asymmetric hydrophilic blocks: synthesis and aqueous solution properties

    Petrov, P; Yoncheva, K. (Krassimira); Mokreva, P. (Pavlina); Konstantinov, S.; J M Irache; Müller, A.H.E. (Axel H.E.)

    2013-01-01

    The synthesis and aggregation behaviour in aqueous media of novel amphiphilic poly(ethylene oxide)- block-poly(n-butyl acrylate)-block-poly(acrylic acid) (PEO–PnBA–PAA) triblock terpolymers were studied. Terpolymers composed of two highly asymmetric hydrophilic PEO (113 monomer units) and PAA (10–17 units) blocks, and a longer soft hydrophobic PnBA block (163 or 223 units) were synthesized by atom transfer radical polymerisation (ATRP) of n-butyl acrylate and tert-butyl acrylate ...

  9. CATALYTIC HYDROGENATION OF ACRYLATE ASMMETRIC Dd(Ⅱ)—CHELATING RESINS CONTAINING AMINO ACID LIGANDS

    Wangying; WangHongzuo; 等

    1995-01-01

    The catalytic hydrogenation of palladium chelating resins containing chiral amino acid ligands based on lower crosslinked poly(chloroethyl acrylate) and some effects on the rate of hydrogenation were studied.

  10. FT-RAMAN SPECTROSCOPY FOR MONITORING THE POLYMERIZATION OF ACRYLIC ACID IN AQUEOUS SOLUTION

    Jiang Yu; Hui-zhou Liu; Jia-yong Chen

    1999-01-01

    FT-Raman spectroscopy was used to monitor the polymerization of acrylic acid in aqueous solution. A simple method to avoid the noise in the background during the signal processing via Fourier transformation was used in this work. The effects of the amount of initiator used on the polymerization are studied. When the amount of the initiator in the polymerization was increased, both the rate and extent of polymerization of acrylic acid will be increased.

  11. Synthesis and Properties of IPN Hydrogels Based on Konjac Glucomannan and Poly(acrylic acid)

    Bing LIU; Zhi Lan LIU; Ren Xi ZHUO

    2006-01-01

    Novel interpenetrating polymer network (IPN) hydrogels based on konjac glucomannan (KGM) and poly(acrylic acid) (PAA) were prepared by polymerization and cross-linking of acrylic acid (AA) in the pre-fabricated KGM gel. The IPN gel was analyzed by FT-IR. The studies on the equilibrium swelling ratio of IPN hydrogels revealed their sensitive response to environmental pH value. The results of in vitro degradation showed that the IPN hydrogels retain the enzymatic degradation character of KGM.

  12. Interaction of photosensitive surfactant with DNA and poly acrylic acid

    In this paper, we investigate interactions and phase transitions in polyelectrolyte-surfactant complexes formed between a cationic azobenzene-containing surfactant and two types of polyelectrolytes: natural (DNA) or synthetic (PAA: poly acrylic acid). The construction of a phase diagram allowed distancing between four major phases: extended coil conformation, colloidally stable compacted globules, colloidal instability range, and surfactant-stabilized compact state. Investigation on the complexes’ properties in different phases and under irradiation with UV light provides information about the role of the surfactant's hydrophobic trans isomers both in the formation and destruction of DNA and PAA globules as well as in their colloidal stabilization. The trans isomer shows much stronger affinity to the polyelectrolytes than the hydrophilic cis counterpart. There is no need for complete compensation of the polyelectrolyte charges to reach the complete compaction. On contrary to the findings previously reported in the literature, we demonstrate – for the first time – complete polyelectrolyte compaction which occurs already at 20% of DNA (and at 50% of PAA) charge compensation. The trans isomer plays the main role in the compaction. The aggregation between azobenzene units in the photosensitive surfactant is a driving force of this process. The decompaction can be realized during UV light irradiation and is strongly influenced by the interplay between surfactant-surfactant and surfactant-DNA interactions in the compacted globules

  13. Radiation grafting of acrylic acid onto polypropylene films

    A study has been made for the preparation of membranes by the direct radiation grafting of acrylic acid (AAc) onto polypropylene (PP) films. The appropriate reaction conditions were selected under which the graft polymerization was carried out successfully. The effect of different solvents such as benzene, methanol/water mixture, isopropanol/water mixture, dimethyl formamide and distilled water on the swelling and grafting process of AAc onto PP films was investigated. In this grafting system ammonium ferrous sulphate (Mohr's salt) and ferric chloride were used as inhibitors to minimize the homopolymerisation of AAc and the suitable concentration of the inhibitor was found to be 1.0 and 1.5 wt% for Mohr's salt and ferric chloride, respectively. Also, the effect of monomer concentration on the rate of grafting was investigated. The dependence of the grafting rate on monomer concentration was found to be 1.1 order. This grafting system proceeded by diffusion controlled process. Some selected properties of the grafted films such as swelling behaviour, gel determination, mechanical and electrical properties were also investigated. It was found that the grafted membranes possess good hydrophilic properties which may make them promising in some practical applications. (author)

  14. Characterization of Functionalized Acrylic acid /4- Vinyl Pyridine Graft Copolymers

    Properties and characterization of the membranes prepared by radiation grafting of acrylic acid (AAc) or/ and 4-vinyl pyridine (4VP) onto low density polyethylene (LDPE) and polypropylene (PP) films were carried out. The FTIR spectra for the grafted membranes were studied to evaluate the structure change as a result of grafting. The swelling behaviour of the graft copolymer in methanol was studied. It was found that the grafting of AAc and/ or 4- VP onto LDPE and PP resulted in introducing good hydrophilic properties to such polymer substrates. The hydrophilic properties were directly proportional to the amount of functional groups. The mechanical properties (Young's modulus, elongation percent and tensile strength) of the grafted membranes also, have been investigated. As the grafting degree increases, the modulus also increases. Increasing the hydrophilicity of the membranes by chemical treatment enhances its mechanical properties. The thermal parameters of the grafted membranes such as δHm1. δHm2, and Trc have been also studied by using DSC

  15. Interaction of photosensitive surfactant with DNA and poly acrylic acid

    Zakrevskyy, Yuriy, E-mail: yuriy.zakrevskyy@fh-koeln.de; Paasche, Jens; Lomadze, Nino; Santer, Svetlana, E-mail: santer@uni-potsdam.de [Experimental Physics, Institute of Physics and Astronomy, University of Potsdam, Karl-Liebknecht-Str. 24-25, D-14476 Potsdam (Germany); Cywinski, Piotr; Cywinska, Magdalena; Reich, Oliver; Löhmannsröben, Hans-Gerd [Physical Chemistry, Institute of Chemistry, University of Potsdam, Karl-Liebknecht-Str. 24-25, D-14476 Potsdam (Germany)

    2014-01-28

    In this paper, we investigate interactions and phase transitions in polyelectrolyte-surfactant complexes formed between a cationic azobenzene-containing surfactant and two types of polyelectrolytes: natural (DNA) or synthetic (PAA: poly acrylic acid). The construction of a phase diagram allowed distancing between four major phases: extended coil conformation, colloidally stable compacted globules, colloidal instability range, and surfactant-stabilized compact state. Investigation on the complexes’ properties in different phases and under irradiation with UV light provides information about the role of the surfactant's hydrophobic trans isomers both in the formation and destruction of DNA and PAA globules as well as in their colloidal stabilization. The trans isomer shows much stronger affinity to the polyelectrolytes than the hydrophilic cis counterpart. There is no need for complete compensation of the polyelectrolyte charges to reach the complete compaction. On contrary to the findings previously reported in the literature, we demonstrate – for the first time – complete polyelectrolyte compaction which occurs already at 20% of DNA (and at 50% of PAA) charge compensation. The trans isomer plays the main role in the compaction. The aggregation between azobenzene units in the photosensitive surfactant is a driving force of this process. The decompaction can be realized during UV light irradiation and is strongly influenced by the interplay between surfactant-surfactant and surfactant-DNA interactions in the compacted globules.

  16. Radiation-induced grafting of acrylic acid onto polypropylene film and its biodegradability

    Mandal, Dev K.; Bhunia, Haripada; Bajpai, Pramod K.; Chaudhari, C. V.; Dubey, K. A.; Varshney, L.

    2016-06-01

    Polypropylene based commodity polyolefins are widely used in packaging, manufacturing, electrical, pharmaceutical and other applications. The aim of the present work is to study the effect of grafting of acrylic acid on the biodegradability of acrylic acid grafted polypropylene. The effect of different conditions showed that grafting percentage increased with increase in monomer concentration, radiation dose and inhibitor concentration but decreased with increase in radiation dose rate. The maximum grafting of 159.4% could be achieved at optimum conditions. The structure of grafted polypropylene films at different degree of grafting was characterized by EDS, FTIR, TGA, DSC, SEM and XRD. EDS studies showed that the increase in acrylic acid grafting percentage increased the hydrophilicity of the grafted films. FTIR studies indicated the presence of acrylic acid on the surface of polypropylene film. TGA studies revealed that thermal stability decreased with increase in grafting percentage. DSC studies showed that melting temperature and crystallinity of the grafted polypropylene films lower than polypropylene film. SEM studies indicated that increase in acrylic acid grafting percentage increased the wrinkles in the grafted films. The maximum biodegradability could be achieved to 6.85% for 90.5% grafting. This suggested that microorganisms present in the compost could biodegrade acrylic acid grafted polypropylene.

  17. Synthesis and characterization of cashew gum/acrylic acid nanoparticles

    Silva, Durcilene A. da; Feitosa, Judith P.A. [Departamento de Quimica Organica e Inorganica, Universidade Federal do Ceara - C. Postal 6021, 60.455-760, Fortaleza, CE (Brazil); Paula, Haroldo C.B. [Departamento de Quimica Analitica e Fisico-Quimica, Universidade Federal do Ceara - C. Postal 6021, 60.455-760, Fortaleza, CE (Brazil); Paula, Regina C.M. de [Departamento de Quimica Organica e Inorganica, Universidade Federal do Ceara - C. Postal 6021, 60.455-760, Fortaleza, CE (Brazil)], E-mail: rpaula@dqoi.ufc.br

    2009-03-01

    This paper describes the preparation of nanoparticles from cashew gum (CG) and acrylic acid (AA) by free radical polymerization using cerium (IV) ammonium nitrate (CAN) as an initiator. The yields of the nanoparticles (NP) obtained by varying the R{sub CG/AA} from 0.5 to 2.0 were between 65 and 40%. The FT-IR spectra of the NP samples showed bands characteristic of the cashew gum spectrum and a new band at 1560 cm{sup -1} assigned to the stretching vibration of COO{sup -} groups of polyacrylic acid. On increasing the R{sub CG/AA} from 0.5 to 2.0 an increase in particle size was observed. The NP with an R{sub CG/AA} of 0.5 were smaller and had higher storage stability than the NP with an R{sub CG/AA} of 1.0 or 2.0. The increase in R{sub CG/AA} had no significant effect on the zeta potential of the NP in water. The NP were dried and re-dissolved in water to observe the effect of freeze-drying on particle size. For the NP with an R{sub CG/AA} of 0.5 an increase in particle size was observed from 71 to 402 nm, however, for the NP with an R{sub CG/AA} of 1.0 or 2.0 a small variation in particle diameter was noted. The behavior of the CG/AA NP was also found to be pH sensitive.

  18. Radiation modification of water absorption of cassava starch by acrylic acid/acrylamide

    Graft co polymerizations of acrylamide and/or acrylic acid onto cassava starch by a simultaneous irradiation technique using gamma-rays as the initiator were studied with regard to various parameters of importance: the monomer-to-cassava starch ratio, total dose (kGy), dose rate (kGy h-1), acrylamide-to-acrylic acid ratio, and the addition of nitric acid and maleic acid as the additives. Grafting parameters were determined in relation to the water absorption of the saponified graft copolymer. The water absorption of the saponified graft copolymer in salt and buffer solutions of different ionic strengths was also measured, from which the super absorbent properties are found to be P H sensitive. The starch graft copolymers of acrylamide and acrylic acid give higher water absorption than the starch graft copolymers of either acrylamide or acrylic acid alone. The porosity of the saponified starch graft copolymers prepared by the acrylamide/acrylic acid ratios of 70:30 and 50:50 was much higher than the porosity of copolymers in terms of fine networks. Ionic strength and multi-oxidation states of the saline and buffer solutions markedly decreased the water absorption of the saponified cassava starch grafted super absorbent polymers.

  19. Polymorphism and polymerisation of acrylic and methacrylic acid at high pressure

    Oswald, Iain D. H.; Urquhart, Andrew J.

    2011-01-01

    The polymorphism and polymerisation of two related acids have been investigated under high pressure conditions. Acrylic acid crystallises as a new polymorph at 0.65 GPa whilst methacrylic acid crystallises in a new polymorph at a higher pressure of 1.5 GPa. Both these new polymorphs exhibit similar...

  20. Radiation sensitive acrylate composition

    This application relates to radiation-sensitive compositions and more particularly to such compositions comprising acrylated esters. As used in this specification, the term acrylated esters refers to either acrylic or methacrylic acid resins. 3 tabs

  1. Gold Nanoparticles Protected with Thiol-Derivatized Amphiphilic Poly( -caprolactone)-b-poly(acrylic acid)

    Javakhishvili, Irakli; Hvilsted, Søren

    2008-01-01

    Amphiphilic poly(c-caprolactone)-b-poly(acrylic acid) (HS-PCL-b-PAA) bearing thiol functionality at the PCL terminal has been synthesized by a combination of ring-opening polymerization (ROP) of c-caprolactone (c-CL), esterification of hydroxy chain end with protected mercaptoacetic acid, subsequ......Amphiphilic poly(c-caprolactone)-b-poly(acrylic acid) (HS-PCL-b-PAA) bearing thiol functionality at the PCL terminal has been synthesized by a combination of ring-opening polymerization (ROP) of c-caprolactone (c-CL), esterification of hydroxy chain end with protected mercaptoacetic acid...

  2. Synthesis of acrylic acid derivatives from carbon dioxide and ethylene mediated by molecular nickel complexes

    Lee, Sin Ying Tina

    2013-01-01

    This work aimed at the synthesis of acrylic acid derivatives from ethylene and CO2 and well as the investigation of β-hydride elimination reaction of nickelalactones with methyl iodide and methyl triflate to form methyl acrylate. The oxidative coupling reaction of ethylene and CO2 on nickel center was ligand selective, and gave low yields of nickelalactone product at mild synthetic conditions. Key intermediates identified and characterized in the β-H elimination reaction provided rich insight...

  3. Enzymatic direct synthesis of acrylic acid esters of mono- and disaccharides

    Tsukamoto, Junko; Heabel, Sophie; Valenca, Gustavo P.; Peter, Martin; Franco, Telma

    2010-01-01

    BACKGROUND: There is an increased need to replace materials derived from fossil sources by renewables. Sugar-cane derived carbohydrates are very abundant in Brazil and are the cheapest sugars available in the market, with more than 400 million tons of sugarcane processed in the year 2007. The objective of this work was to study the preparation of sugar acrylates from free sugars and free acrylic acid, thus avoiding the previous preparation of protected sugar derivatives, such as glycosides, o...

  4. Acidic polyanion poly(acrylic acid) prevents calcium oxalate crystal deposition

    Kleinman, Jack G.; Alatalo, Laura J.; Beshensky, Ann M.; Wesson, Jeffrey A.

    2008-01-01

    Acidic macromolecules inhibit calcium oxalate nucleation, growth, aggregation and attachment to cells in vitro. To test for such an effect in vivo we used osmotic minipumps to continuously infuse several doses of the 5.1 kDa poly(acrylic acid) (pAA5.1) into rats fed a diet which causes renal calcium oxalate crystal deposition. Although kidneys of rats receiving the saline control contained calcium oxalate crystals, measured by polarized light microscopy, those of animals given pAA5.1 had sign...

  5. Graft Polymerization of Acrylic Acid on a Polytetrafluoroethylene Panel by an Inductively Coupled Plasma

    Lan, Yan; You, Qingliang; Cheng, Cheng; Zhang, Suzhen; Ni, Guohua; Nagatsu, M.; Meng, Yuedong

    2011-02-01

    Surface modification on a polytetrafluoroethylene (PTFE) panel was performed with sequential nitrogen plasma treatments and surface-initiated polymerization. By introducing COO- groups to the surface of the PTFE panel through grafting polymerization of acrylic acid (AA), a transparent poly (acrylic acid) (PAA) membrane was achieved from acrylic acid solution. Grafting polymerization initiating from the active groups was achieved on the PTFE panel surface after the nitrogen plasma treatment. Utilizing the acrylic acid as monomers, with COO- groups as cross link sites to form reticulation structure, a transparent poly (acrylic acid) membrane with arborescent macromolecular structure was formed on the PTFE panel surface. Analysis methods, such as fourier transform infrared spectroscopy (FTIR), microscopy and X-ray photoelectron spectroscopy (XPS), were utilized to characterize the structures of the macromolecule membrane on the PTFE panel surface. A contact angle measurement was performed to characterize the modified PTFE panels. The surface hydrophilicities of modified PTFE panels were significantly enhanced after the plasma treatment. It was shown that the grafting rate is related to the treating time and the power of plasma.

  6. EB curable coating based on soy-oil fatty acid modified acrylate

    Soy-oil fatty acid was used to synthesize the soy-oil fatty acid modified acrylic coating by esterification reaction. After coating and EB curing, the results showed that the properties of the film were excellent, and it was suitable for the coating of wood furniture cured by EB

  7. Effects of preirradiation graft polymerization of acrylic acid onto polyethylene film

    With the aid of preirradiation method of grafting onto low-density polyethylene film, a systematic investigation was made of grafting of aqueous acrylic acid under conditions such as monomer concentrations, irradiation dose, dose rate, reaction time, the effect of concentrations of Mohr's salt and sulphuric acid on the graft reaction. (author)

  8. Direct Synthesis of Hyperbranched Poly(acrylic acid-co-3-hydroxypropionate

    Efkan Çatıker

    2015-01-01

    Full Text Available Hyperbranched poly(acrylic acid-co-3-hydroxypropionate (PAcHP was synthesized by base-catalyzed hydrogen transfer polymerization of acrylic acid through one step. The copolymers obtained through solution and bulk polymerization were insoluble in water and all organic solvents tried. Structural and compositional characterizations of hyperbranched PAcHP were performed by using FTIR, solid 13C-NMR, TGA, and titrimetric analysis. Acrylate fraction of the hyperbranched PAcHP obtained via bulk polymerization was determined as 60–65% by comparing TGA curves of hyperbranched PAcHP and pure poly(3-hydroxy propionate (PHP. However, analytical titration of the same sample revealed that acrylic acid units were about 47.3%. The results obtained from TGA and analytical titration were used to evaluate the chemical structure of the copolymer. Hyperbranched PAcHP exhibited hydrogel properties. Swelling behavior of the copolymer was investigated at a wide pH range and ionic strength. The dynamic swelling profiles of hyperbranched PAcHP exhibited a fast swelling behavior in the first hour and achieved the equilibrium state within 12 h in PBS. Depending on the conditions, the copolymers exhibited swelling ratios up to 2100%. As the copolymer has easily biodegradable propionate and versatile functional acrylic acid units, it can be used as not only biodegradable material in medical applications but also raw material in personal care commodities.

  9. Effects of acrylamide and acrylic acid on creatine kinase activity in the rat brain

    In vitro, both acrylamide and acrylic acid inhibited creatine kinase (CK) activity in rat brain homogenates, and acrylic acid was more potent than acrylamide. In vivo, however, when given i.p. 50 mg/kg per day for 8 days to rats, only acrylamide inhibited CK activity in the brain and caused apparent neurological signs. 14C in the brain 24 h after the injection of 14C-labelled chemicals was more than 7 times greater with acrylamide than with acrylic acid. The inhibition of CK activity by acrylamide varied in eight regions of the brain; from 54% in hypothalamus to 27% in cerebellar vermis. The regional difference of CK inhibition, however, did not agree well with either 14C distribution or with the distribution in regions which appear clinically or pathologically vulnerable to acrylamide. (orig.)

  10. Preparation and characteristics of acrylic acid/styrene composite plasma polymerized membranes

    Plasma polymerization has gained increasing interest for the deposition of functional plasma-polymerized membranes suitable for a wide range of applications on account of its advantageous features. In this work, acrylic acid/styrene composite plasma polymerized membranes were synthesized by plasma polymerization of a mixture of acrylic acid and styrene monomers in a low-frequency after-glow capacitively coupled plasma (CCP) discharge process. The structure and composition of the plasma polymerized membranes were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The results showed that the partial pressure ratio between acrylic acid (AA) and styrene (St), applied discharge power and the energy of the extracted particles have considerable effects on the structure and the content of functional groups of the deposited membranes.

  11. Effects of gas atmospheres on poly(lactic acid) film in acrylic acid plasma treatment

    Plasma polymerized acrylic acid (AA) coatings were deposited on poly(lactic acid) (PLA) films in various gas atmospheres during the pre-treatment of PLA and the deposition of AA, respectively. Therefore, this work was twofold: the argon pretreated PLA films followed by a deposition in argon were investigated against the mixture of argon and oxygen pretreated ones under the same deposition conditions; the plasma deposition of AA operating in different atmospheres (argon, oxygen and nitrogen) was employed to modify the pretreated PLA in oxygen. Chemical and physical changes on the plasma-treated surfaces were examined using contact angle, X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FE-SEM) and attenuated total reflection infrared (ATR-FTIR) analysis. The results showed that the discharge gas can have a significant influence on the chemical composition of the PLA surfaces: oxygen plasmas introduced oxygen-containing groups in company with surface etching in pretreatment and deposition, while argon discharges was able to achieve much better hydrophilic behavior and high retention ratio of poly(acrylic acid) (PAA) coating before and after washing in water.

  12. Effects of gas atmospheres on poly(lactic acid) film in acrylic acid plasma treatment

    Zhao, Yun, E-mail: yun.zhaotju@yahoo.com [Dipartimento di Scienza Applicata e Tecnologia, Politecnico di Torino, C.so Duca degli Abruzzi 24, 10129 Turin (Italy); Fina, Alberto [Dipartimento di Scienza Applicata e Tecnologia, Politecnico di Torino – sede di Alessandria, V. T. Michel 5, 15121 Alessandria (Italy); Venturello, Alberto; Geobaldo, Francesco [Dipartimento di Scienza Applicata e Tecnologia, Politecnico di Torino, C.so Duca degli Abruzzi 24, 10129 Turin (Italy)

    2013-10-15

    Plasma polymerized acrylic acid (AA) coatings were deposited on poly(lactic acid) (PLA) films in various gas atmospheres during the pre-treatment of PLA and the deposition of AA, respectively. Therefore, this work was twofold: the argon pretreated PLA films followed by a deposition in argon were investigated against the mixture of argon and oxygen pretreated ones under the same deposition conditions; the plasma deposition of AA operating in different atmospheres (argon, oxygen and nitrogen) was employed to modify the pretreated PLA in oxygen. Chemical and physical changes on the plasma-treated surfaces were examined using contact angle, X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FE-SEM) and attenuated total reflection infrared (ATR-FTIR) analysis. The results showed that the discharge gas can have a significant influence on the chemical composition of the PLA surfaces: oxygen plasmas introduced oxygen-containing groups in company with surface etching in pretreatment and deposition, while argon discharges was able to achieve much better hydrophilic behavior and high retention ratio of poly(acrylic acid) (PAA) coating before and after washing in water.

  13. A study on antithrombogenic polymeric dialytic membrane. Irradiation grafting acrylic acid and styrene into polyethylene films

    A new type of antithrombogenic polymeric dialytic membrane with a hydrophilic-hydrophobic microphase structure was prepared by grafting acrylic acid and styrene into polyethylene films, using peroxidation pre-irradiation technique. Various ratios of monomers influencing on properties of the grafted films were examined. Experimental results showed that the grafted films have superior mechanic strength, and their antithrombogenicity and permeability were 30 and 10 times higher than that of the ungrafted films respectively on condition of the volume ratio 1:1 (styrene vs acrylic acid)

  14. The influence of Copolimers Acrylic Acid onto Poli(Etilene Terephthalate)woven fabric

    To improve suitability of wearing poli etilene terephthalate (PET) wovenfabric, it need to enhance the ability in absorbing of water vapour. For theabove reason acrylic acid (AA) has been grafted onto PET wovenfabric(PET-g-AA). Fourier Transform Infrared (FT-IR) data show that poly(acrylic acid) have grafted onto PET woven fabric. Thermal propertiesobtained from DSC (Differential Scanning Calorimeter) measurements of PET-g-AA show that the grafting does not affect bulk properties of PET. Thedecrease of the tensile strength had occurred to PET-g-MMA, however it ratherinfluenced by the reaction time than the initial concentration of acrylicacid. (author)

  15. Synthesis of Acrylic Acid/Kaoline Powder Superabsorbent Composite by Inverse-suspending Polymerization

    ZHONG Jin-feng; XUE Yi-ming; WU Ji-huai; LIN Jian-ming; WEI Yue-lin

    2004-01-01

    An acrylic acid/kaoline powder superabsorbent composite with a water absorbency of the superabsorbent composite about 1/800 was synthesized by inverse-suspending polymerization reaction between acrylic acid monomer and kaoline ultrafine powder. The influence of the dispersant agent on the configuration of the products in the inverse suspension polymerization is investigated. The influences of the kaoline powder, cross-linker, initiator, neutralization degree and the volume ratio of oil to water phase on the water absorbency of the superabsorbent composites are discussed in the paper.

  16. Graft Copolymerization of Acrylic Acid onto Fungal Cell Wall Structural Polysaccharide

    2001-01-01

    Acrylic acid was graft-copolymerized onto Rhi. oryzae's cell wall structural polysacchaxide directly and efficiently in aqueous solution with ceric ammonium nitrate as initiator. The maximal grafting percentage of 135.5% was obtained under the condition of [Ce4+]=5mmol.L-1, [AA]=1mol.L-1, T=60°C and t=3h. Graft copolymerization was suggested to proceed through free radical reaction mechanism. Grafting occurred primarily on chitosan. Acrylic acid was also attempted to be grafted onto Asp. niger cell wall structural polysaccharide, and only 44.2% of grafting percentage was resulted.

  17. Electroactive behavior assessment of poly(acrylic acid)-graphene oxide composite hydrogel in the detection of cadmium

    Bejarano-Jimenez, A.; Escobar-Barrios, V.A.; Kleijn, J.M.; Oritz-Ledon, C.A.; Chazaro-Ruiz, L.F.

    2014-01-01

    Super absorbent polymers of acrylic acid-graphene oxide (PAA-GO) were synthesized with different percentage of chemical neutralization (0, 10, and 20%) of the acrylic acid monomer before its polymerization. The influence of their swelling and adsorption/desorption capacity of cadmium ions in aqueous

  18. SYNTHESIS OF 2—HYDROXYETHYL ACRYLATE BY USING STRONG ACIDIC CATION ION EXCHANGE RESIN AS CATALYST

    GAODabin

    1992-01-01

    2-Hydroxyethyl acrylate is synthesized from acrylic acid and ethylene glycol under a simple and mild condition by using strong acidic cation ion exchange resin as a catalyst,which could be recycled as long as 10 times with high activation.

  19. Poly(acrylic acid) to induce competitive crystallization of a theophylline/oxalic acid cocrystal and a theophylline polymorph

    Jang, Jisun; Kim, Il Won

    2016-01-01

    Polymeric additives to induce competitive crystallization of pharmaceutical compounds were explored. A cocrystal of theophylline and oxalic acid was used as a model system, and poly(acrylic acid), poly(caprolactone), and poly(ethylene glycol) were the additives. The cocrystal formation was selectively hindered with addition of poly(acrylic acid). First the size of the cocrystals were reduced, and eventually the cocrystallization was inhibited to generate neat theophylline crystals. The theophylline crystals were of a distinctively different crystal structure from known polymorphs, based on powder X-ray diffraction. They were also obtained in nanoscale size, when millimeter-scale crystals formed without poly(acrylic acid). Polymeric additives that could form specific interactions with crystallizing compounds seem to be useful tools for the phase and size control of pharmaceutical crystals.

  20. The preparation nad water absorption of a copolymer from konjac-graft-acrylic acid by irradiation

    The konjac and acrylic acid were grafted by 4.0kGy 60Co γ-rays irradiation. The water absorption property of copolymers was studied. The results showed that the optimum feed ratio was konjac powder: acrylic acid: NaOH (9.5mol/L):water=3g: 21ml: 17.8ml: 131ml. And the optimum reation conditions: volume/mass ratio of acrylic acid and konjac was 7:1, neutralization degree of acrylic acid was 55%, gel drying temperature was 30 degree C. The copolymer particle size of 40 ∼ 80 mesh had the largest absorption of water, up to 886.5 times at room temperature. The water-absorption and water-holding capabilities were affected by temperature, and were better at the termperater lower than 60 degree C. The water absorption was also affected by pH and ion concentration of solution, and the ion concentration was the main factor. The largest water absorption at Na2HPO4 - citric acid buffer was only 15.8% of which in distilled water at the optimum pH=6. (authors)

  1. Selective oxidation of propane to acrylic acid over mixed metal oxide catalysts

    Wei Zheng; Zhenxing Yu; Ping Zhang; Yuhang Zhang; Hongying Fu; Xiaoli Zhang; Qiquan Sun; Xinguo Hu

    2008-01-01

    The effects of metal atomic ratio, water content, oxygen content, and calcination temperature on the catalytic perfor-mances of MoVTeNbO mixed oxide catalyst system for the selective oxidation of propane to acrylic acid have been investigated and discussed. Among the catalysts studied, it was found that the MoVTeNbO catalyst calcined at a temperature of 600 ℃ showed the best performance in terms of propane conversion and selectivity for acrylic acid under an atmosphere of nitrogen. An effective MoVTeNbO oxide catalyst for propane selective oxidation to acrylic acid was obtained with a combination of a preferred metal atomic ratio (Mo1 V0.31Te0.23Nb0.12). The optimum reaction condition for the selective oxidation of propane was the molar ratio of C3H81 :O2 : H2O : N1 = 4.4 : 12.8 : 15.3 : 36.9. Under such conditions, the conversion of propane and the maximum yield of acrylic acid reached about 50% and 21%, respectively.

  2. Gold Nanoparticles Protected with Thiol-Derivatized Amphiphilic Poly(epsilon-caprolactone)-b-poly(acrylic acid)

    Javakhishvili, Irakli; Hvilsted, Søren

    2009-01-01

    Amphiphilic poly(epsilon-caprolactone)-b-poly(acrylic acid) (HS-PCL-b-PAA) with a thiol functionality in the PCL terminal has been prepared in a novel synthetic cascade. Initially, living anionic ring-opening polymerization (ROP) of epsilon-caprolactone (epsilon-CL) employing the difunctional...

  3. Extraction Equilibrium of Acrylic Acid by Aqueous Two-Phase Systems Using Hydrophilic Ionic Liquids

    As an effective method for extraction of acrylic acid, aqueous two-phase systems based on morpholinium ionic liquids were used in this study. Effects of the alkyl chain length of cation in morpholinium ionic liquids on phase diagram and extraction efficiencies were investigated. Experimental results show that aqueous two phase systems can be formed by adding appropriate amount of morpholinium ionic liquids to aqueous K2HPO4 solutions. It can be found that the ability of morpholinium ionic liquids for phase separation followed the order [HMMor][Br]>[OMMor][Br]>[BMMor][Br]>[EMMor][Br]. There was little difference between binodal curves of imidazolium ionic liquids and those of morpholinium ionic liquids. 50-90% of the extraction efficiency was observed for acrylic acid by aqueous two phase extraction of acrylic acid with morpholinium ionic liquids. It can be concluded that morpholinium ionic liquids/K2HPO4 were effective for aqueous two phases extraction of acrylic acid comparing to imidazolium ionic liquids/K2HPO4 systems because of their lower cost

  4. Depletion of abundant plasma proteins by poly(N-isopropylacrylamide-acrylic acid) hydrogel particles

    Such-Sanmartín, Gerard; Ventura-Espejo, Estela; Jensen, Ole N

    2014-01-01

    the application of pH-sensitive poly(N-isopropylacrylamide-acrylic acid) hydrogel particles for removal of abundant plasma proteins, prior to proteome analysis by MS. Protein depletion occurs by two separate mechanisms: (1) hydrogel particles incubated with low concentrations of plasma capture...

  5. Monitor of Polymerization of Inverse Microemulsions Containing Methyl Methacrylate and Acrylic Acid

    Xiao LI; Sheng Ping XIA; Wei Jie ZENG; Wei Ying ZHANG; Sheng Xiong DONG

    2006-01-01

    The polymerization of the inverse microemulsions composed of methyl methacrylate,acrylic acid, sodium dodecyl sulfate and water was monitored by refractometer, conductometer and time-resolved light scattering device. The results showed that refractive index, conductivity or intensity distribution of scattered light changed along with polymerization, and different processes of polymerization could be identified.

  6. Adsorption of uranium ions by crosslinked polyester resin functionalized with acrylic acid from aqueous solutions

    In this paper, the crosslinked polyester resin containing acrylic acid functional groups was used for the adsorption of uranium ions from aqueous solutions. For this purpose, the crosslinked polyester resin of unsaturated polyester in styrene monomer (Polipol 353, Poliya) and acrylic acid as weight percentage at 80 and 20%, respectively was synthesized by using methyl ethyl ketone peroxide (MEKp, Butanox M60, Azo Nobel)-cobalt octoate initiator system. The adsorption of uranium ions on the sample (0.05 g copolymer and 5 mL of U(VI) solution were mixed) of the crosslinked polyester resin functionalized with acrylic acid was carried out in a batch reactor. The effects of adsorption parameters of the contact time, temperature, pH of solution and initial uranium(VI) concentration for U(VI) adsorption on the crosslinked polyester resin functionalized with acrylic acid were investigated. The adsorption data obtained from experimental results depending on the initial U(VI) concentration were analyzed by the Freundlich, Langmuir and Dubinin-Radushkevich (D-R) adsorption isotherms. The adsorption capacity and free energy change were determined by using D-R isotherm. The obtained experimental adsorption data depending on temperature were evaluated to calculate the thermodynamic parameters of enthalpy (ΔHo), entropy (ΔSo) and free energy change (ΔGo) for the U(VI) adsorption on the crosslinked polyester resin functionalized with acrylic acid from aqueous solutions. The obtained adsorption data depending on contact time were analyzed by using adsorption models such as the modified Freundlich, Elovich, pseudo-first order and pseudo-second-order kinetic models. (author)

  7. Cisplatin-incorporated nanoparticles of poly(acrylic acid-co-methyl methacrylate copolymer

    Lee KD

    2013-08-01

    Full Text Available Kyung Dong Lee,1,* Young-Il Jeong,2,* Da Hye Kim,3,4 Gyun-Taek Lim,2 Ki-Choon Choi5 1Department of Oriental Medicine Materials, Dongshin University, Naju, South Korea; 2Department of Polymer Engineering, Chonnam National University, Gwangju, South Korea; 3Faculty of Life and Environmental Science, Shimane University, Matsue, Japan; 4United Graduate School of Agricultural Sciences, Tottori University, Tottori, Japan; 5Grassland and Forages Division, National Institute of Animal Science, Rural Development Administration, Cheonan, South Korea *These authors contributed equally to this work Background: Although cisplatin is extensively used in the clinical field, its intrinsic toxicity limits its clinical use. We investigated nanoparticle formations of poly(acrylic acid-co-methyl methacrylate (PAA-MMA incorporating cisplatin and their antitumor activity in vitro and in vivo. Methods: Cisplatin-incorporated nanoparticles were prepared through the ion-complex formation between acrylic acid and cisplatin. The anticancer activity of cisplatin-incorporated nanoparticles was assessed with CT26 colorectal carcinoma cells. Results: Cisplatin-incorporated nanoparticles have small particle sizes of less than 200 nm with spherical shapes. Drug content was increased according to the increase of the feeding amount of cisplatin and acrylic acid content in the copolymer. The higher acrylic acid content in the copolymer induced increase of particle size and decrease of zeta potential. Cisplatin-incorporated nanoparticles showed a similar growth-inhibitory effect against CT26 tumor cells in vitro. However, cisplatin-incorporated nanoparticles showed improved antitumor activity against an animal tumor xenograft model. Conclusion: We suggest that PAA-MMA nanoparticles incorporating cisplatin are promising carriers for an antitumor drug-delivery system. Keywords: cisplatin, nanoparticle, poly(acrylic acid-co-methyl methacrylate, ion complexes

  8. Grafting of acrylic acid onto polytetrafluoroethylene (PTFE) micropowder via pre-irradiation

    Grafting of acrylic acid (AAc) onto the surface of PTFE micropowder was performed by pre-irradiation method, in order to improve their dispersion in aqueous solution.The effects of various experimental parameters on the degree of grafting(G) were separately investigated, including: volume fraction of AAc, proper addition of concentrated sulfuric acid, mass fraction of inhibitor and reaction time. The result shows that G is increasing with increment of AAc concentration below 50%, and can be enhanced by adding a proper amount of sulfuric acid. Under our experimental conditions, G reached its saturated value when the mass concentration of the inhibitor was 0.8 g/L and the reaction time was 3 h. The introduction of more than 10% of poly(acrylic acid) chain on PTFE micropowder results in the good dispersion of PTFE micropowder in aqueous NaOH solution. (authors)

  9. CHARACTERIZATION OF RADIATION GRAFTING DEGREE OF POLYSTYRENE g-ACRYLIC ACID BY XPS

    CHE Jitai; ZHANG Wanxi

    1990-01-01

    It this work, characterization of radiation grafting degree of polystyrene-g-acrylic acid by XPS was studied. It is found that along with the main peak C1s there is a photoelectron peak at 289.0 eV that appears to be C1s of -C(=O)-OH group and shows the presence ofpolyacrylic acid grafted on the polystyrene.The grafting degree obtained by XPS is in agreement with that from the gravimetric method.

  10. Oxidative dehydration of glycerol to acrylic acid over vanadium-impregnated zeolite beta

    Pestana, Carolina F.M.; Guerra, Antonio C.O.; Turci, Cassia C. [Universidade Federal do Rio de Janeiro, RJ (Brazil). Inst. de Quimica; Ferreira, Glaucio B. [Universidade Federal Fluminense, Niteroi, RJ (Brazil). Inst. de Quimica; Mota, Claudio J.A., E-mail: cmota@iq.ufrj.br [INCT Energia e Ambiente, Universidade Federal do Rio de Janeiro, RJ (Brazil)

    2013-01-15

    The oxidative dehydration of glycerol to acrylic acid was studied over vanadium-impregnated zeolite Beta. Catalysts were prepared by wet impregnation of ammonium metavanadate over ammonium-exchanged zeolite Beta, followed by air calcination at 823 K. Impregnation reduced the specific surface area, but did not significantly affected the acidity (Bronsted and Lewis) of the zeolites. The catalytic evaluation was carried out in a fixed bed flow reactor using air as the carrier and injecting glycerol by means of a syringe pump. Acrolein was the main product, with acetaldehyde and hydroxy-acetone (acetol) being also formed. Acrylic acid was formed with approximately 25% selectivity at 548 K over the impregnated zeolites. The result can be explained by XPS (X-ray photoelectron spectroscopy) measurements, which indicated a good dispersion of the vanadium inside the pores. (author)

  11. Properties of radiation curable hyperbranched polyurethane acrylate from palm oil oleic acid

    Radiation curable hyperbranched urethane acrylate (HBPUA) from oleic acid of palm oil was synthesized aided by p-toluene sulfonic acid as a catalyst. This mixture was then used as the core (HBP-1) and reacted with palm oil oleic acid to form the hyperbranched polyol (HBP-2). HBPUA was prepared by reacting HBP-2 resin with diisocyanate and hydroxyl-containing acrylate monomer with the presence of 0.1-2 wt% dibutyltin dilaurate as a catalyst. The reaction was confirmed by several analytical data i.e. hydroxyl value (OHV), Fourier Transform infrared (FT IR) spectroscopy gel permeation chromatography (GPC) and nuclear magnetic resonance (NMR) spectroscopy analyses. The HBPUA was easily curable when subjected to electron beam (EB) or ultraviolet (UV) radiation. (authors)

  12. Oxidative dehydration of glycerol to acrylic acid over vanadium-impregnated zeolite beta

    The oxidative dehydration of glycerol to acrylic acid was studied over vanadium-impregnated zeolite Beta. Catalysts were prepared by wet impregnation of ammonium metavanadate over ammonium-exchanged zeolite Beta, followed by air calcination at 823 K. Impregnation reduced the specific surface area, but did not significantly affected the acidity (Bronsted and Lewis) of the zeolites. The catalytic evaluation was carried out in a fixed bed flow reactor using air as the carrier and injecting glycerol by means of a syringe pump. Acrolein was the main product, with acetaldehyde and hydroxy-acetone (acetol) being also formed. Acrylic acid was formed with approximately 25% selectivity at 548 K over the impregnated zeolites. The result can be explained by XPS (X-ray photoelectron spectroscopy) measurements, which indicated a good dispersion of the vanadium inside the pores. (author)

  13. Superabsorbent biphasic system based on poly(lactic acid) and poly(acrylic acid)

    Sartore, Luciana; Pandini, Stefano; Baldi, Francesco; Bignotti, Fabio

    2016-05-01

    In this research work, biocomposites based on crosslinked particles of poly(acrylic acid), commonly used as superabsorbent polymer (SAP), and poly-L-lactic acid (PLLA) were developed to elucidate the role of the filler (i.e., polymeric crosslinked particles) on the overall physico-mechanical behavior and to obtain superabsorbent thermoplastic products. Samples prepared by melt-blending of components in different ratios showed a biphasic system with a regular distribution of particles, with diameter ranging from 5 to 10 μm, within the PLLA polymeric matrix. The polymeric biphasic system, coded PLASA i.e. superabsorbent poly(lactic acid), showed excellent swelling properties, demonstrating that cross-linked particles retain their superabsorbent ability, as in their free counterparts, even if distributed in a thermoplastic polymeric matrix. The thermal characteristics of the biocomposites evidence enhanced thermal stability in comparison with neat PLLA and also mechanical properties are markedly modified by addition of crosslinked particles which induce regular stiffening effect. Furthermore, in aqueous environments the particles swell and are leached from PLLA matrix generating very high porosity. These new open-pore PLLA foams, produced in absence of organic solvents and chemical foaming agents, with good physico-mechanical properties appear very promising for several applications, for instance in tissue engineering for scaffold production.

  14. Determination of acrylamide and acrylic acid by isocratic liquid chromatography with pulsed electrochemical detection.

    Casella, Innocenzo G; Pierri, Marianna; Contursi, Michela

    2006-02-24

    The electrochemical behaviour of the polycrystalline platinum electrode towards the oxidation/reduction of short-chain unsaturated aliphatic molecules such as acrylamide and acrylic acid was investigated in acidic solutions. Analytes were separated by reverse phase liquid chromatographic and quantified using a pulsed amperometric detection. A new two-step waveform, is introduced for detection of acrylamide and acrylic acid. Detection limits (LOD) of 20 nM (1. 4 microg/kg) and 45 nM (3.2 microg/kg) were determined in water solutions containing acrylamide and acrylic acid, respectively. Compared to the classical three-step waveform, the proposed two-step waveform shows favourable analytical performance in terms of LOD, linear range, precision and improved long-term reproducibility. The proposed analytical method combined with clean-up procedure accomplished by Carrez clearing reagent and subsequent extraction with a strong cation exchanger cartridges (SPE), was successfully used for the quantification of low concentrations of acrylamide in foodstuffs such as coffee and potato fries. PMID:16426623

  15. Nanoparticles of Block Ionomer Complexes from Double Hydrophilic Poly(acrylic acid-b-poly(ethylene oxide-b-poly(acrylic acid Triblock Copolymer and Oppositely Charged Surfactant

    Sun Yuelong

    2009-01-01

    Full Text Available Abstract The novel water-dispersible nanoparticles from the double hydrophilic poly(acrylic acid-b-poly(ethylene oxide-b-poly(acrylic acid (PAA-b-PEO-b-PAA triblock copolymer and oppositely charged surfactant dodecyltrimethyl ammonium bromide (DTAB were prepared by mixing the individual aqueous solutions. The structure of the nanoparticles was investigated as a function of the degree of neutralization (DN by turbidimetry, dynamic light scattering (DSL,ζ-potential measurement, and atomic force microscope (AFM. The neutralization of the anionic PAA blocks with cationic DTAB accompanied with the hydrophobic interaction of alkyl tails of DTAB led to formation of core–shell nanoparticles with the core of the DTAB neutralized PAA blocks and the shell of the looped PEO blocks. The water-dispersible nanoparticles with negative ζ-potential were obtained over the DN range from 0.4 to 2.0 and their sizes depended on the DN. The looped PEO blocks hindered the further neutralization of the PAA blocks with cationic DTAB, resulting in existence of some negative charged PAA-b-PEO-b-PAA backbones even when DN > 1.0. The spherical and ellipsoidal nature of these nanoparticles was observed with AFM.

  16. Preparation of poly (acrylic acid)-modified chitosan amphiphilic gels by γ-rays irradiation

    Poly (acrylic acid)-modified chitosan amphiphilic gels were prepared via O-maleoyl-N-phthaloyl- chitosan as an intermediate by grafting with poly (acrylic acid). The reaction was carried out in a homogeneous sys- tem by γ-ray irradiation. Evidence of grafting was obtained from FTIR spectroscopy. The effects for grafting reaction were investigated systematically. Results show that the grafting degree depends on monomer concentration and ab- sorbed dose. The swelling behavior of chitosan samples with different grafting degree was studied in different buffers as a function of pH. It can be found that all the samples swollen slightly at low pH but very well at high pH. More- over, the swelling behavior of chitosan samples in DMF has been evaluated. (authors)

  17. Removal of Dyes from Aqueous Solutions Using Radiation Synthesized (2-Hydroxyethyl Methacrylate/Acrylic acid) Hydrogels

    Acrylic acid/2-hydroxyethyl methacrylate super absorbent hydrogels (AAc/ HEMA) were prepared by γ-radiation copolymerization of 2-hydroxyethyl methacrylate (HEMA) and acrylic acid (AAc). Characterization of AAc/HEMA hydrogel was done by FTIR, TGA, SEM and XRD. The swelling properties were studied as a function of time, ph and irradiation dose. The diffusion behavior of water into these hydrogels followed the Fickian character at all investigated irradiation doses. The adsorption of Direct Congo Red and Direct Blue dyes onto the AAc/ HEMA hydrogel was studied. Physico-chemical parameters like dye concentration, solution ph and temperature were varied to characterize the adsorption phenomenon. Experimental data were modeled by Freundlich isotherm. Thermodynamic parameters ( ΔHo, ΔGo and ΔSo ) were evaluated for the dyes adsorbent systems, which suggest that the adsorption process is a typical physical process and endothermic in nature

  18. Preparation of poly(acrylic acid) particles by dispersion polymerization in an ionic liquid.

    Minami, Hideto; Kimura, Akira; Kinoshita, Keigo; Okubo, Masayoshi

    2010-05-01

    Poly(acrylic acid) (PAA) particles were successfully prepared by dispersion polymerization of acrylic acid in ionic liquid, N,N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoro-methanesulfonyl)amide ([DEME][TFSA]) at 70 degrees C with low hydrolysis grade (35.4%) poly(vinyl alcohol) as stabilizer. Interestingly, the PAA particles were easily extracted as particle state with water. Thus, the PAA particles had a cross-linked structure during the polymerization without cross-linker. Moreover, it was also noted that the cross-linking density of the PAA particles could be controlled by thermal treatment at various temperatures in [DEME][TFSA] utilizing the advantages of nonvolatility and high thermal stability of the ionic liquid. PMID:20043688

  19. Super absorbent Prepared by Radiation Induced Graft Copolymerization of Acrylic Acid onto Cassava Starch

    Full text: Super absorbent was synthesized by radiation-induced graft polymerization of acrylic acid onto cassava starch. Parameters such as the absorbed dose and the amount of monomer were investigated in order to determine the optimum conditions for the grafting polymerization. Water retention, germination percentage and germination energy were determined in order to evaluate the possibility of super absorbent in agricultural applications, especially in arid regions. The graft copolymer was characterized by FTIR. Results indicated that the sand mixed with 0.1%wt super absorbent can absorb more water than the sand without super absorbent. The germination energy of corn seeds mixed with 0.5% super absorbent was obviously higher than those without super absorbent. These experimental results showed that the super absorbent has considerable effect on seed germination and the growth of young plants. Keywords: Super absorbent, Radiation, Acrylic acid, Cassava starch

  20. Pre-irradiation induced emulsion co-graft polymerization of acrylonitrile and acrylic acid onto a polyethylene nonwoven fabric

    A pre-irradiation induced emulsion co-graft polymerization method was used to introduce acrylonitrile and acrylic acid onto a PE nonwoven fabric. The use of acrylic acid is meant to improve the hydrophilicity of the modified fabric. The kinetics of co-graft polymerization were studied. The existence of polyacrylonitrile (PAN) and poly(acrylic acid) (PAAc) graft chains was proven by Fourier transform infrared spectroscopy (FTIR) analysis. The existence of the nitrile groups in the graft chains indicates that they are ready for further amidoximation and adsorption of heavy metal ions. - Highlights: • Acrylonitrile and acrylic acid were co-grafted onto a PE nonwoven fabric. • Pre-irradiation induced emulsion graft polymerization technique is applied. • The existence of AAc resulted in the increased hydrophilicity of the grafted fabric

  1. Preparation and evaluation of chitosan-poly (acrylic acid hydrogels as stomach specific delivery for amoxicillin and metronidazole

    Hemant Yadav K

    2007-01-01

    Full Text Available The objective of the present work was to develop stomach specific delivery systems for amoxicillin and metronidazole using chitosan and poly(acrylic acid hydrogels. Chitosan and poly(acrylic acid hydrogels were prepared with different composition of copolymers. The hydrogels were evaluated for swelling studies, mucoadhesive studies, in vitro drug release, scanning electron microscopic and FTIR analysis. The effect of chitosan and poly (acrylic acid on swelling and in vitro drug release was carried out. The n value calculated was < 0.5 for all the formulations containing amoxicillin and metronidazole indicating Fickian diffusion mechanism. The hydrogels with chitosan and poly (acrylic acid ratio of 0.25:1 showed greater mucoadhesive property, maximum swelling and complete release of drugs, hence can be used for stomach specific delivery of drugs.

  2. Flocculation Efficiency of Poly(Acrylamide-Co-Acrylic Acid) Obtained by Electron Beam Irradiation

    Gabriela Craciun; Elena Manaila; Maria-Daniela Stelescu

    2013-01-01

    A correlation between physicochemical characteristics of flocculants obtained by electron beam irradiation and their efficiency for wastewater treatment is presented. For real wastewater treatment, our interest was focused upon total suspended solids, fatty matter, and chemical oxygen demand. Flocculation studies were carried out using a standard jar test. A treatment option based on poly(acrylamide-co-acrylic acid) for wastewater taken from a slaughterhouse plant is presented.

  3. Modification of hydrophobic polypeptide-based film by blending with hydrophilic poly(acrylic acid)

    Guoquan Zhu; Fagang Wang; Qiaochun Gao; Yuying Liu

    2013-01-01

    In this study, a series of poly(γ-benzyl L-glutamate)/poly(acrylic acid) (PBLG/PAA) polymer blend films were prepared by casting the polymer blend solution in dimethylsulfoxide (DMSO). The structure and morphology of the polymer blend film were investigated by Fourier Transform Infrared Spectroscopy (FT-IR) and Scanning Electron Microscopy (SEM). Thermal, mechanical, and chemical properties of PBLG/PAA polymer blend films were studied by Differential Scanning Calorimetry (DSC), Thermogra...

  4. Investigation on the Inverse Emulsion Polymerization of Acrylic Acid

    2002-01-01

    Polyacrylic acid particles in nano-scale were synthesized using an inverse (W/O) emulsion polymerization method. The particle size and size change of inverse micelles which solubilize a part of monomer solution was monitored by PCS (photon correlation spectroscopy) and the particles of polyacrylic acid were viewed in scanning electron microscope for the first time. It was concluded that the inverse micelles were primarily the polymerization reaction sites.

  5. Synthesis and characterization of kappaphycus seaweed-poly (acrylic) acid superabsorbent hydrogel for agricultural use

    The main objective of this research is to synthesize and characterize kappaphycus seaweed-poly (acrylic) acid superabsorbent hydrogel for agricultural use. The superabsorbent polymers (SAPs), KCSW: PAA hydrogels were synthesized by using gamma radiation technique from Cobalt-60 source at absorbed dose 0f 5, 10 and 15 kGy. The effect of absorbed dose, seaweed concentration, and concentration of acrylic acid on the degree of swelling was studied and optimum swelling conditions were established. Irradiated samples of 3% KCSW, 50% neutralized AAC at an absorbed dose of 10kGy gave the highest degree of swelling and gel fraction and were found to be suitable for application in the agriculture. Samples with different concentrations of acrylic acid were characterized using FTIR and TGA. The water retention experiment in sandy soil showed high water retention capacity of KCSW: PAA hydrogel at a value of 92% for a period of 7 days. Effect of the germination of mung bean showed very promising result of 78% germination.(author)

  6. Swelling of Bacterial Cellulose-Acrylic Acid Hydrogels: Sensitivity Towards External Stimuli

    This study evaluated various environmental factors affecting the swelling degree of bacterial cellulose-acrylic acid hydrogels. Aqueous bacterial cellulose-acrylic acid (4:1) mixtures were prepared and subjected to electron beam irradiation at 30 and 50 kGy. Swelling rate under influenced of pH, temperature and ionic strength was investigated from 1 to 24 hours. Swelling degree of hydrogels was dependent on irradiation dose: those synthesized at 50 kGy exhibited significant higher swelling degree (p<0.0001) in methanol (619 %) compared to water (510 %) at room temperature after 24 hours. External ionic strength affected swelling, for example elevation in sodium chloride concentration decreased swelling degree. Hydrogels were also sensitive to pH: swelling increased with increasing pH and was optimal at pH 7. Swelling also increased with increasing temperature from 25 to 50 degree Celsius. In conclusion, the ability of electron irradiated bacterial cellulose-acrylic acid hydrogels to respond to various external environment make it a material to be developed as an active delivery system for drugs, proteins and hormones. (author)

  7. Influence of ozone and paracetic acid disinfection on adhesion of resilient liners to acrylic resin

    2016-01-01

    PURPOSE The aim of this study was to evaluate the effect of paracetic acid (PAA) and ozone disinfection on the tensile bond strength (TBS) of silicone-based resilient liners to acrylic resins. MATERIALS AND METHODS One hundred and twenty dumbbell shaped heat-polymerized acrylic resins were prepared. From the mid segment of the specimens, 3 mm of acrylic were grinded off and separated parts were reattached by resilient liners. The specimens were divided into 2 control (control1, control7) and 4 test groups of PAA and ozone disinfection (PAA1, PAA7, ozone1 and ozone7; n=10). While control groups were immersed in distilled water for 10 min (control1) and 7 days (control7), test groups were subjected to PAA (16 g/L) or ozone rich water (4 mg/L) for 1 cycle (10 min for PAA and 60 min for ozone) per day for 7 days prior to tensile tests. Measurements of the TBS were analyzed using 3-way ANOVA and Tukey's HSD test. RESULTS Adhesive strength of Mollosil decreased significantly by application of ozone disinfection. PAA disinfection had no negative effect on the TBS values of Mollosil and Molloplast B to acrylic resin. Single application of ozone disinfection did not have any negative effect on TBS values of Molloplast B, but prolonged exposure to ozone decreased its adhesive strength. CONCLUSION The adhesion of resilient liners to acrylic was not adversely affected by PAA disinfection. Immersion in ozonated water significantly decreased TBS of Mollosil. Prolonged exposure to ozone negatively affects adhesion of Molloplast B to denture base materials. PMID:27555898

  8. Impact of Acrylic Acid on ASP Flooding Performance: Interfacial Tension Behaviour

    Shuaib Ahmed Kalwar

    2014-01-01

    Full Text Available In chemical EOR, interfacial tension plays one of the important roles in carbonate reservoirs. Carbonate reservoirs are composed of calcium and magnesium minerals which affect the performance of alkali and surfactants to reduce interfacial tension. In this study, acrylic acid was used to inhibit precipitation and to create a compatible solution without any precipitations. The impact of acrylic acid on interfacial tension was investigated using various inhibitor concentrations with a hard brine composition of 59, 940 TDS. Sodium metaborate, alpha olefin sulfonate and internal olefin sulfonate were screened as promising chemicals for interfacial tension. Various fluid-fluid compatibility tests were first performed to find the optimum acid-alkali ratio to prevent any precipitations. The optimum acid-alkali ratio was found to be 0.6:1.0. This ratio was then used to keep all solution without any precipitations for 30 days at 80°C. It was also observed that the increase in acid-alkali concentrations can significantly reduce the interfacial tension. Using the optimum concentration for acid, alkali and surfactant, the interfacial tension reduced from 14.9-0.401 mN m-1.

  9. Structure and Proton Conductivity in Mixtures of Poly(acrylic acid) and Imidazole

    Yang, Han-Chang; Griffin, Philip J.; Winey, Karen I.; University of Pennsylvania Team

    2015-03-01

    Proton conductivity in polymer electrolyte membranes (PEMs) typically involves water, which requires that during operation the humidity of the PEM be carefully controlled. In contrast, anhydrous protic polymer membranes promote proton transport by incorporating heterocyclic molecules, such as imidazole and its derivatives, into acid-containing polymers. In this work, we explore the interplay between nanoscale-structure and proton conduction of poly(acrylic acid) (PAA) blended at varying compositions with 2-ethyl-4-methylimidazole (EMI). We present the glass transition temperature from differential scanning calorimetry, morphology characterization from X-ray scattering, and proton conductivity from electrical impedance spectroscopy.

  10. The active component of vanadium-molybdenum catalysts for the oxidation of acrolein to acrylic acid

    The catalytic properties of the vanadium-molybdenum oxide system were investigated in the oxidation of acrolein to acrylic acid. The active component of the catalyst is the compound VMo3O11, the maximum amount of which is observed at a content of 7-15 mole% V2O4. The compound VMo3O11 is formed in the thermodecomposition of silicomolybdovanadium heteropoly acids or isopoly compounds, reduced with respect to vanadium, and contains V4+ and Mo6+. The optimum treatment for the formation of this compound is treatment in the reaction mixture at 400 degrees C

  11. ESTERIFICATION OF ACRYLIC ACID WITH 1-BUTANOL IN LIQUID PHASE CATALYZED WITH AL-MCM-41

    Edson Avellaneda Maytán; Gustavo Paim Valença

    2010-01-01

    This work studies the esterification of acrylic acid with 1-butanol using Al-MCM-41 as catalyst with different degrees of acidity at different temperatures. Al-MCM-41 synthesis was made from bromate Cetyl trimethyl ammonium using as router agent, NH4OH (25%), deionized H2O and Al2(SO4)3. Catalytic tests were carried out by groups and worked with temperature ranges among (333 to 348) K and a small sample was collected at predetermined intervals of time for subsequent gas chromatography analysi...

  12. Ultra-Thin Films of Poly(acrylic acid)/Silver Nanocomposite Coatings for Antimicrobial Applications

    Alaa Fahmy; Eisa, Wael H.; Mohamed Yosef; Ali Hassan

    2016-01-01

    In this work not only colloids of poly(acrylic acid) (PAA) embedded with silver nanoparticles (Ag-NPs) but thin films (10 nm) also were deposited using electrospray deposition technique (ESD). A mixture of sodium borohydride (NaBH4) and ascorbic acid (AA) were utilized to reduce the silver ions to generate Ag-NPs in the PAA matrix. Moreover, sodium tricitrate was used to stabilize the prepared colloids. The obtained colloids and films were characterized using UV-visible, transmission electron...

  13. Bioinspired bioadhesive polymers: dopa-modified poly(acrylic acid) derivatives.

    Laulicht, Bryan; Mancini, Alexis; Geman, Nathanael; Cho, Daniel; Estrellas, Kenneth; Furtado, Stacia; Hopson, Russell; Tripathi, Anubhav; Mathiowitz, Edith

    2012-11-01

    The one-step synthesis and characterization of novel bioinspired bioadhesive polymers that contain Dopa, implicated in the extremely adhesive byssal fibers of certain gastropods, is reported. The novel polymers consist of combinations of either of two polyanhydride backbones and one of three amino acids, phenylalanine, tyrosine, or Dopa, grafted as side chains. Dopa-grafted hydrophobic backbone polymers exhibit as much as 2.5 × the fracture strength and 2.8 × the tensile work of bioadhesion of a commercially available poly(acrylic acid) derivative as tested on live, excised, rat intestinal tissue. PMID:23008096

  14. Partial oxidation of D-xylose to maleic anhydride and acrylic acid over vanadyl pyrophosphate

    Xylose is the second most abundant sugar after glucose. Despite its tremendous potential to serve as a renewable feedstock, few commercial processes exploit this resource. Here, we report a new technology in which a two-fluid nozzle atomizes a xylose-water solution into a capillary fluidized bed operating above 300 °C. Xylose-water droplets form at the tip of the injector, vaporize then react with a heterogeneous mixed oxide catalyst. A syringe pump metered the solution to the reactor charged with 1 g of catalyst. Product yield over vanadyl pyrophosphate was higher compared to molybdenum trioxide-cobalt oxide and iron molybdate; it reached 25% for maleic anhydride, 17% for acrylic acid and 11% for acrolein. Gas residence time was 0.2 s. The catalyst was free of coke even after operating for 4 h – based on a thermogravimetric analysis of catalyst withdrawn from the reactor. Below 300 °C, powder agglomerated at the tip of the injector at 300 °C; it also agglomerated with a xylose mass fraction of 7% in water. - Highlights: • D-xylose reacts to form maleic anhydride and acrylic acid above 250 °C. • Vanadyl pyrophosphate is both active and selective for maleic and acrylic acid. • Acid and acrolein yield approaches 50% for a xylose mass fraction of 3% in water. • Catalyst agglomerates at low temperatures and high xylose aqueous mass fraction. • Atomization quality is a determining factor to minimize agglomeration

  15. Antibacterial activity of chitosan and the interpolyelectrolyte complexes of poly(acrylic acid-chitosan

    Hortensia Ortega-Ortiz

    2010-06-01

    Full Text Available The antimicrobial activity of chitosan and water soluble interpolyelectrolyte complexes of poly(acrylic acid-chitosan was studied. Chitosans of two different molecular weights were tested at different concentration for 0.5 to 5 g·L-1 as antimicrobial agents against P. aeruginosa and P. oleovorans. In both cases, the best microbial inhibition was obtained with the concentration of 5 g·L-1. However, the interpolyelectrolyte complexes of poly(acrylic acid-chitosan with composition φ =2 produced higher antibacterial activity than the two chitosans at the concentration of 0.5 g·L-1. The NPEC2 complex was more effective than chitosans. This could be attributed to the number of moles of the amino groups of chitosan and the carboxylic acid groups of the interpolyelectrolyte complexes poly(acrylic acid.A atividade antimicrobiana de quitosana e complexos interpolieletrolíticos hidrossoluvéis de poli(ácido acrílico-quitosana foi estudada. Quitosanas de dois diferentes pesos moleculares foram testados em diferentes concentrações, 0,5 a 5 g • L-1, como agentes antimicrobianos nas P. aeruginosa e P. oleovorans. Em ambos os casos, obteu-se a melhor inibição microbiana com a concentração de 5 g • L-1, no entanto os complexos interpolieletrolíticos de poli (ácido acrílico-quitosana com composição φ = 2 apresentaram maior atividade antibacteriana do que os dois quitosans na concentração de 0,5 g • L-1. O complexo NPEC2 foi mais eficaz do que as quitosanas, sendo que o resultado pode ser atribuído ao número de moles dos grupos aminos da quitosana e aos grupos carboxílicos dos complexos de poli(ácido acrílico.

  16. Synthesis of superabsorbent hydrogel by radiation crosslinking of acrylic acid, semi-refined kappa-carrageenan and sugarcane bagasse blend

    Superabsorbent hydrogels have three-dimensional networks that enable it to exhibit great water absorption capacity leading to its promising applications. However, existing commercial hydrogels are mainly acrylic acid which causes environmental problems. In this study, the incorporation of agricultural waste as filler and polysaccharide from natural sources as binder for the production of superabsorbent hydrogel was done to reduce the use of acrylic acid as well as its environmental impact while adding value to the incorporated materials. A series of superabsorbent hydrogel with the blend of acrylic acid, semi-refined kappa carrageenan and sugarcane bagasse were synthesized by radiation crosslinking. The gel fraction and swelling capacity of the hydrogels were determined and studied. The characterizations were facilitated by Fourier transform infrared spectroscopy technique (FTIR) and Thermogravimetric Analysis (TGA). In the results obtained from analyses, the characteristic peaks of acrylic acid and sugarcane bagasse were observed in the FTIR spectra and the three step peaks if synthesized hydrogel in its TGA implies an improvement in thermal stability of the product. The synthesized superabsorbent hydrogel blends had exhibited comparable gel fraction to that of the polyacrylic acid hydrogel, had great swelling capacity, and achieved equilibrium degree of swelling within 72-96 hours. The optimum synthesized superabsorbent hydrogel is 3% semi-refined kappa-carrageenan, 3% sugarcane bagasse, 15% acrylic acid neutralize up to 50% and irradiated at 15kGy dose which exhibited a swelling of 599.53 and gel fraction of 39.73. (author)

  17. Use of acrylic acid in the synthesis of molecularly imprinted polymers for the analysis of cyproheptadine

    The synthesis and comparative characterization of molecularly imprinted polymers (MIPs) with cyproheptadine (CYP), using two different monomers, acrylic acid (AA) and methacrylic acid (MAA), are described. Polyacids (PA) [poly(methacrylic acid) (PMAA) and poly(acrylic acid) (PAA)] were obtained by the radical polymerization of MAA and AA, respectively, in dichloromethane as the porogen solvent-imprinted medium. The non-covalent imprinting process was performed via thermal decomposition of an azo-initiator at 60 deg. C, using ethylene glycol dimethacrylate as the cross-linker and 2,2'-azobis(2-methylpropionitrile) as the initiator. The selectivities of MIPs and NIPs particles were evaluated in binding experiments of the four synthesized polymeric materials (MIPaa, MIPmaa, NIPmaa and NIPaa) with CYP. The effects of monomers on: a) the surface morphology, b) the binding capacity and c) the swelling properties of imprinted and non-imprinted polymers were studied and are presented here. Polymer material morphology was assessed with scanning electron microscopy (SEM). This revealed differences in monomer function, depending on which one was employed, as well as differences in function when polymerization occurred in the presence of template or without it. Non-specific retention of the template to NIPs was higher for NIPs-PAA polymers than for NIPs-PMAA materials. In terms of specific binding (ΔQ = QMIP - QNIP), MIPmaa showed the greatest value (53.47%) in comparison with MIPaa (50.07%)

  18. Synthesis of acrylic prepolymer

    An acrylic prepolymer was synthesized from glycidyl methacrylate (GMA), butyl methacrylate (BMA), methyl methacrylate (MMA) and acrylic acid (AA). Butyl acetate (BAc), benzoyl peroxide (BzO), 4-methoxyphenol (MPh) and triethylamine (TEA) were used as solvent, initiator, inhibitor and catalyst respectively. Observations of the synthesis leading to the formation of acrylic prepolymer are described. (author)

  19. Physicochemical and electrochemical characterization of battery separator prepared by radiation induced grafting of acrylic acid onto microporous polypropylene membranes

    2009-05-01

    Full Text Available Mutual radiation grafting technique was used to graft acrylic acid on micrometer thick micro-porous polypropylene membrane using high-energy gamma radiation. Grafting could not be achieved in aqueous acrylic acid solution. The presence of Mohr’s salt effectively retarded the homopolymerization of acrylic acid but did not lead to grafting enhancement. Mohr’s salt in presence of acids was found to be effective in enhancing the grafting yield. Contact angle measurement studies of the grafted and radiation treated polypropylene showed that initial grafting as well as radiation treatment of poly(propylene in aqueous medium and in presence of Mohr’s salt enhances its affinity towards the grafting solution. The enhancement in the polar component of surface energy of treated polypropylene membrane is the primary cause of grafting enhancement. The membranes grafted to an extent of ~20% were found to perform comparably with the battery separator presently being used by battery industry.

  20. Modification of magnetite coating formation in presence of alkaline acrylic acid

    In Indian PHWR's, the hot conditioning of primary heat transport system is carried out to form a protective magnetite coating on the inner surface of PHT system at the start up of the reactor and also after decontamination of PHT system to minimize the release of loose crud particulates and corrosion of the PHT system. An attempt has been made to modify the chemistry conditions for the formation of protective magnetite coating on CS coupons in a static autoclave at 523K to view its impact on the nature of the protectivity. In continuation of our efforts to modify the film with various organic additives like Glycerol, Ethylene glycol, PEG, in this paper the effect of acrylic acid on magnetite coating formation is discussed. The metal oxide powders synthesized by polymer combustion route in PVA, PEG and PAA resulted in nano crystallites. To see the effect of theses organics in reducing the crystallite sizes and improving the corrosion resistance behaviour in hydrothermal conditions the experiments are carried out. In presence of Acrylic acid (AA) at different concentrations (50, 100, 500ppm) at alkaline pH (LiOH -10.4 ) in static autoclave, magnetite coating is formed on CS coupons. The coupons were characterized by XRD, SEM, Raman and Electrochemical impedance and Potentiodynamic Anodic Polarization (PDAP) studies. The addition of acrylic acid results in smaller crystallite sizes and the crystallites look like thread bundles for 50ppm concentration of AA. PDAP studies indicate better film protectivity for magnetite coating formed in 50 ppm AA. Corrosion rate is observed to be less for CS coupons in presence of 50 and 100 ppm AA. The tendency for the film formed to dissolve is less for both 50 and 100 ppm AA developed coating in comparison to coating developed in LiOH alone. The impedance studies indicated the pore resistance of the film increased two fold and seven fold for 50 and 100 ppm acrylic acid case in comparison to simple LiOH case where as the charge

  1. Modification of hydrophobic polypeptide-based film by blending with hydrophilic poly(acrylic acid

    Guoquan Zhu

    2013-01-01

    Full Text Available In this study, a series of poly(γ-benzyl L-glutamate/poly(acrylic acid (PBLG/PAA polymer blend films were prepared by casting the polymer blend solution in dimethylsulfoxide (DMSO. The structure and morphology of the polymer blend film were investigated by Fourier Transform Infrared Spectroscopy (FT-IR and Scanning Electron Microscopy (SEM. Thermal, mechanical, and chemical properties of PBLG/PAA polymer blend films were studied by Differential Scanning Calorimetry (DSC, Thermogravimetric (TG Analysis, Tensile Tests, and measurements of Surface Contact Angles. The results revealed that the introduction of PAA could exert great effects on the structure and properties of the polypeptide films.

  2. Synthesis of hemicellulose-acrylic acid graft copolymer super water absorbent resin by ultrasonic irradiation technology

    Liu, Fangfang; Conghui DU; Linya ZHANG

    2015-01-01

    The hemicellulose super water absorbent resin is prepared by using ultrasonic irradiation technology, with the waste liquid produced during the preparation of viscose fiber which contains a large amount of hemicellulose as raw material, acrylic acid as graft monomer, N,N’-methylene bis acrylamide (NMBA) as cross linking agent, and (NH4)2S2O8-NaHSO3 as the redox initiation system. The synthesis conditions, structure and water absorption ability of resin are discussed. The results indicate that...

  3. Novel Routes for the Design of Poly((meth)acrylic acid) Containing Polymer Structures by Controlled Radical Polymerization

    Van Camp, W

    2007-01-01

    Easy preparation of specialty polymers containing poly((meth)acrylic acid) Poly(acrylic acid) (PAA) and poly(methacrylic acid) (PMAA) are well-known polymers in a high number of applications because of their pH-responsive nature, their hydrophylic characteristics and for their interaction with metal ions. PAA, high tech material An increasing part of high tech polymer materials introduce P(M)AA as segments in well-defined polymer structures. These can be block copolymers, polymer brushes, sta...

  4. Characterization of bioactive RGD peptide immobilized onto poly(acrylic acid) thin films by plasma polymerization

    Seo, Hyun Suk; Ko, Yeong Mu; Shim, Jae Won [Department of Dental Materials, School of Dentistry, MRC Center, Chosun University, Gwangju (Korea, Republic of); Lim, Yun Kyong; Kook, Joong-Ki [Department of Oral Biochemistry, School of Dentistry, Chosun University, Gwangju (Korea, Republic of); Cho, Dong-Lyun [School of Applied Chemical Engineering and Center for Functional Nano Fine Chemicals, Chonnam National University, Gwangju (Korea, Republic of); Kim, Byung Hoon, E-mail: kim5055@chosun.ac.kr [Department of Dental Materials, School of Dentistry, MRC Center, Chosun University, Gwangju (Korea, Republic of)

    2010-11-01

    Plasma surface modification can be used to improve the surface properties of commercial pure Ti by creating functional groups to produce bioactive materials with different surface topography. In this study, a titanium surface was modified with acrylic acid (AA) using a plasma treatment and immobilized with bioactive arginine-glycine-aspartic acid (RGD) peptide, which may accelerate the tissue integration of bone implants. Both terminals containing the -NH{sub 2} of RGD peptide sequence and -COOH of poly(acrylic acid) (PAA) thin film were combined with a covalent bond in the presence of 1-ethyl-3-3-dimethylaminopropyl carbodiimide (EDC). The chemical structure and morphology of AA film and RGD immobilized surface were investigated by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR), atomic force microscopy (AFM), and scanning electron microscopy (SEM). All chemical analysis showed full coverage of the Ti substrate with the PAA thin film containing COOH groups and the RGD peptide. The MC3T3-E1 cells were cultured on each specimen, and the cell alkaline phosphatase (ALP) activity were examined. The surface-immobilized RGD peptide has a significantly increased the ALP activity of MC3T3-E1 cells. These results suggest that the RGD peptide immobilization on the titanium surface has an effect on osteoblastic differentiation of MC3T3-E1 cells and potential use in osteo-conductive bone implants.

  5. Characterization of bioactive RGD peptide immobilized onto poly(acrylic acid) thin films by plasma polymerization

    Plasma surface modification can be used to improve the surface properties of commercial pure Ti by creating functional groups to produce bioactive materials with different surface topography. In this study, a titanium surface was modified with acrylic acid (AA) using a plasma treatment and immobilized with bioactive arginine-glycine-aspartic acid (RGD) peptide, which may accelerate the tissue integration of bone implants. Both terminals containing the -NH2 of RGD peptide sequence and -COOH of poly(acrylic acid) (PAA) thin film were combined with a covalent bond in the presence of 1-ethyl-3-3-dimethylaminopropyl carbodiimide (EDC). The chemical structure and morphology of AA film and RGD immobilized surface were investigated by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR), atomic force microscopy (AFM), and scanning electron microscopy (SEM). All chemical analysis showed full coverage of the Ti substrate with the PAA thin film containing COOH groups and the RGD peptide. The MC3T3-E1 cells were cultured on each specimen, and the cell alkaline phosphatase (ALP) activity were examined. The surface-immobilized RGD peptide has a significantly increased the ALP activity of MC3T3-E1 cells. These results suggest that the RGD peptide immobilization on the titanium surface has an effect on osteoblastic differentiation of MC3T3-E1 cells and potential use in osteo-conductive bone implants.

  6. Characterization of bioactive RGD peptide immobilized onto poly(acrylic acid) thin films by plasma polymerization

    Seo, Hyun Suk; Ko, Yeong Mu; Shim, Jae Won; Lim, Yun Kyong; Kook, Joong-Ki; Cho, Dong-Lyun; Kim, Byung Hoon

    2010-11-01

    Plasma surface modification can be used to improve the surface properties of commercial pure Ti by creating functional groups to produce bioactive materials with different surface topography. In this study, a titanium surface was modified with acrylic acid (AA) using a plasma treatment and immobilized with bioactive arginine-glycine-aspartic acid (RGD) peptide, which may accelerate the tissue integration of bone implants. Both terminals containing the -NH2 of RGD peptide sequence and -COOH of poly(acrylic acid) (PAA) thin film were combined with a covalent bond in the presence of 1-ethyl-3-3-dimethylaminopropyl carbodiimide (EDC). The chemical structure and morphology of AA film and RGD immobilized surface were investigated by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR), atomic force microscopy (AFM), and scanning electron microscopy (SEM). All chemical analysis showed full coverage of the Ti substrate with the PAA thin film containing COOH groups and the RGD peptide. The MC3T3-E1 cells were cultured on each specimen, and the cell alkaline phosphatase (ALP) activity were examined. The surface-immobilized RGD peptide has a significantly increased the ALP activity of MC3T3-E1 cells. These results suggest that the RGD peptide immobilization on the titanium surface has an effect on osteoblastic differentiation of MC3T3-E1 cells and potential use in osteo-conductive bone implants.

  7. Controlled release of anti-diabetic drug Gliclazide from poly(caprolactone)/poly(acrylic acid) hydrogels.

    Bajpai, S K; Chand, Navin; Soni, Shweta

    2015-01-01

    Drug Gliclazide (Glz) has limited solubility and low bioavailability. In order to obtain a controlled release of this drug and to improve its bioavailability, the drug has been loaded into poly(caprolactone) (PCL)/poly(acrylic acid) (PAAc) hydrogels, prepared by free radical polymerization of acrylic acid in the presence of poly(caprolactone) in acetone medium using azo-isobutyronitrile as initiator and N,N' methylene bisacrylamide as cross-linking agent. The swelling behaviour of these hydrogels has been investigated in the physiological gastric and intestinal fluids to obtain an optimum composition suitable for delivery of a biologically active compound. The gels were loaded with anti-diabetic drug Glz and a detailed investigation of release of drug has been carried out. Various kinetic models have been applied on the release data. Finally, the Albino wistar rats were treated for Streptozotocin plus nicotinamide - induced diabetes using a Glz-loaded PCL/PAAc hydrogel. The results indicated a fair reduction in the glucose level of rats. PMID:26135033

  8. Radiation synthesis of chitosan beads grafted with acrylic acid for metal ions sorption

    Benamer, S., E-mail: benamers@yahoo.fr [Division of Nuclear Applications, Centre de Recherche Nucleaire d' Alger, BP-399 Alger-Gare (Algeria); Mahlous, M.; Tahtat, D.; Nacer-Khodja, A.; Arabi, M. [Division of Nuclear Applications, Centre de Recherche Nucleaire d' Alger, BP-399 Alger-Gare (Algeria); Lounici, H.; Mameri, N. [Ecole Nationale Polytechnique d' El-Harrach Alger (Algeria)

    2011-12-15

    Radiation-induced grafting of acrylic acid onto chitosan beads was performed in solution at a dose rate of 20.6 Gy/min of cobalt-60 gamma rays. The effect of absorbed dose on grafting yield was investigated. The characterization of the grafted material was performed by FTIR spectroscopy and the swelling measurements at different pHs. The grafting yield increased with the increase in dose, it reached 80% at 40 kGy irradiation dose. The removal of Pb and Cd ions from aqueous solutions was investigated with both ungrafted and grafted chitosan beads. The sorption behavior of the sorbents was examined through pH, kinetics and equilibrium measurements. Grafted chitosan beads presented higher sorption capacity for both metal ions than unmodified chitosan beads. - Highlights: > Pb and Cd ions are removed from aqueous solution by adsorption on chitosan beads. > Crosslinking process improves chemical stability of chitosan beads. > Radiation grafting of acrylic acid onto chitosan improves its metal adsorption capacity. > Increase in grafting degree enhances the adsorption capacity of the material. > Gamma radiation is a powerful tool for an accurate control of the grafting yield.

  9. Synthesis of ion exchange membrane by radiation grafting of acrylic acid onto polyethylene

    Radiation grafting of vinyl monomers onto polymer films has been extensively studied by many workers. In the preirradiation method of grafting a polymer substrate is activated by irradiation (either in the presence or absence of oxygen) and subsequently allowed to react with a monomer. The preirradiation method was utilized in this study to synthesize an ion exchange membrane useful for a battery separator by grafting acrylic acid onto polyethylene film. The battery separator should be chemically and thermally stable, sufficiently durable in electrolyte as well as highly electrically conductive. Membranes made from regenerated cellulose, e.g., cellophane, have long been used as a separator in the batteries with alkaline electrolyte, such as silver oxide primary cell. However, it has poor durability, as short as one year, due to breakdown of the membrane during operation or storing. The acrylic acid-grafted polyethylene film was found to be quite useful for a separator in the alkaline batteries. This membrane has a high electric conductivity and an excellent durability. (author)

  10. Spectroscopic and density functional theory studies of trans-3-(trans-4-imidazolyl)acrylic acid

    Arjunan, V.; Remya, P.; Sathish, U.; Rani, T.; Mohan, S.

    2014-08-01

    The structural parameters, thermodynamic properties and vibrational frequencies of the optimised geometry of trans-3-(trans-4-imidazolyl)acrylic acid have been determined from B3LYP methods with 6-311++G** and cc-pVTZ basis sets. The effects of substituents (acrylyl group) on the imidazole vibrational frequencies are analysed. The vibrational frequencies of the fundamental modes of trans-3-(trans-4-imidazolyl)acrylic acid have been precisely assigned and analysed and the theoretical results are compared with the experimental vibrations. 1H and 13C NMR isotropic chemical shifts are calculated and the assignments made are compared with the experimental values. The energies of important MO’s of the compound are also determined from DFT method. The total electron density and electrostatic potential of the compound are determined by natural bond orbital analysis. Various reactivity and selectivity descriptors such as chemical hardness, chemical potential, softness, electrophilicity, nucleophilicity and the appropriate local quantities employing natural population analysis (NPA) are calculated.

  11. Antimicrobial and Thermal Properties of Metal Complexes of Grafted Fabrics with Acrylic Acid by Gamma Irradiation

    Cotton, cotton/PET blend and PET fabrics were treated against microbial effect by radiation - induced grafting of acrylic acid followed by metal complexation with some divalent transition metal ions Co (II), Ni (II) and Cu (II). The microbial resistance was evaluated by testing the mechanical properties of the treated fabrics after burring for one and two weeks in a moist soil reach with microorganisms. Also, the growth of microorganisms was examined by scanning electron microscope (SEM). Moreover, the effect of this treatment on the thermal decomposition behavior was investigated by thermogravimetric analysis (TGA). On the basis of microbial studies, it was found that the metal complexation of the grafted fabrics with acrylic acid enhanced the antimicrobial resistance of the fabrics and the antimicrobial resistance could be arranged according to the metal ions as follows: copper> nickel> cobalt. Also, the thermal stability of different fabrics could be arranged as follow: grafted fabrics complexed with Cu (II) > grafted fabrics complexed with Ni (II) > grafted fabrics complexed with Co (II)

  12. Protein absorption and fouling on poly(acrylic acid)-graft-polypropylene microfiltration membrane

    Liu, Yanjun; Ma, Huiying; Lv, Chunying; Yang, Jia; Fu, Xueqi

    2009-07-01

    A series of pH-sensitive poly (acrylic acid)-graft-polypropylene hollow fiber microfiltration membranes were prepared by UV-photo-irradiation. Bovine serum albumin (BSA) was chosen as the model protein to investigate its absorption and fouling behaviors on membranes. The results showed that the hydrophilicity of grafted membrane was improved by poly(acrylic acid) chains with parts of membrane pores blocked. The grafted membranes were markedly pH-dependent on the water permeability as pH was altered from 1 to 11. The zeta potential of grafted membranes calculated by streaming potential was negative in most pH range. Electrostatic interaction energy calculated by DLVO theory showed the electric interaction force between grafted membrane and BSA was attractive. With the rise of grafting degree, the electric attractive force between grafted membrane and BSA increased as pH=3 and decreased as pH=8, while it kept basically unchanged as pH=4.7. As a result, most serious fouling was observed as pH=4.7. Grafted membranes had a lower BSA absorption and better antifouling behavior as pH=8, while the opposite result was revealed as pH=3. In conclusion, the absorption and fouling behavior of BSA on membranes was pH-dependent due to the pH-dependence of membrane charge, and the conformation of BSA and grafting chains.

  13. Investigation of small molecular weight poly(acrylic acid) adsorption on γ-alumina

    Liu, Lei; Luo, Shi-Zhong [College of Chemical Engineering, Sichuan University, Chengdu, Sichuan 610065 (China); Wang, Bin, E-mail: bin_wang@scu.edu.cn [College of Chemical Engineering, Sichuan University, Chengdu, Sichuan 610065 (China); Guo, ZhanHu [Chemical and Biomolecular Engineering Department, University of Tennessee, Knoxville, TN 37996 (United States)

    2015-08-01

    Highlights: • Small molecular weight poly(acrylic acid) incorporated on γ-alumina. • PAA adsorbed primarily on outer surface of alumina at low pH. • PAA infiltrated inside alumina pore at high pH. • Polymer chain reptation motion during the infiltration. - Abstract: The interactions between poly(acrylic acid) (PAA) and alumina have been widely investigated. In this study, the pattern of small molecular weight PAA (M{sub W} 3000) interaction with γ-alumina has been dissected. The alumina/PAA hybrids were prepared at pH 4.0, 5.5, and 7.0, respectively. Nitrogen absorption–desorption analysis, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, and elemental analysis were conducted to illustrate the characteristics of the hybrids. At pH 4.0, the coiled PAA conformation yielded polymer adsorption primarily on alumina outer surface. At higher pH values, the more stretched PAA molecules were able to infiltrate inside the alumina pores. The phenomenon is explained by the polymer chain reptation motion model. Coiled polymer chains are not oriented enough to penetrate the oxide pore channels. In contrary, stretched polymer chains are more likely to move along the pore channels.

  14. Investigation of small molecular weight poly(acrylic acid) adsorption on γ-alumina

    Highlights: • Small molecular weight poly(acrylic acid) incorporated on γ-alumina. • PAA adsorbed primarily on outer surface of alumina at low pH. • PAA infiltrated inside alumina pore at high pH. • Polymer chain reptation motion during the infiltration. - Abstract: The interactions between poly(acrylic acid) (PAA) and alumina have been widely investigated. In this study, the pattern of small molecular weight PAA (MW 3000) interaction with γ-alumina has been dissected. The alumina/PAA hybrids were prepared at pH 4.0, 5.5, and 7.0, respectively. Nitrogen absorption–desorption analysis, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, and elemental analysis were conducted to illustrate the characteristics of the hybrids. At pH 4.0, the coiled PAA conformation yielded polymer adsorption primarily on alumina outer surface. At higher pH values, the more stretched PAA molecules were able to infiltrate inside the alumina pores. The phenomenon is explained by the polymer chain reptation motion model. Coiled polymer chains are not oriented enough to penetrate the oxide pore channels. In contrary, stretched polymer chains are more likely to move along the pore channels

  15. Radiation synthesis of chitosan beads grafted with acrylic acid for metal ions sorption

    Radiation-induced grafting of acrylic acid onto chitosan beads was performed in solution at a dose rate of 20.6 Gy/min of cobalt-60 gamma rays. The effect of absorbed dose on grafting yield was investigated. The characterization of the grafted material was performed by FTIR spectroscopy and the swelling measurements at different pHs. The grafting yield increased with the increase in dose, it reached 80% at 40 kGy irradiation dose. The removal of Pb and Cd ions from aqueous solutions was investigated with both ungrafted and grafted chitosan beads. The sorption behavior of the sorbents was examined through pH, kinetics and equilibrium measurements. Grafted chitosan beads presented higher sorption capacity for both metal ions than unmodified chitosan beads. - Highlights: → Pb and Cd ions are removed from aqueous solution by adsorption on chitosan beads. → Crosslinking process improves chemical stability of chitosan beads. → Radiation grafting of acrylic acid onto chitosan improves its metal adsorption capacity. → Increase in grafting degree enhances the adsorption capacity of the material. → Gamma radiation is a powerful tool for an accurate control of the grafting yield.

  16. Surface properties of ionomers based on styrene-b-acrylic acid copolymers obtained by copolymerization in emulsion

    Surface properties of styrene-b-acrylic acid copolymers obtained in emulsion and suitable ionomers before and after UV-irradiation were studied by measurements of contact angles and FTIR-ATR spectroscopy. The research focused on the influence of different content of carboxylic acid groups in copolymers, of various types and contents of alkali metal salts in ionomers and of cesium acrylate or methacrylate in ionomers on hydrophilicity of the surfaces of these samples and the course of photodegradation in them. Hydrophilicity of initial copolymer surfaces was higher than this of polystyrene as a result of presence of carboxylic acid groups, which also made the surfaces of these copolymers more sensitive to UV-irradiation. Hydrophilicity of the surfaces of ionomers containing cesium acrylates depended on the content of cesium salt in the samples. The course of ionomer photooxidation was also dependent on the content of this salt. The surface of ionomer containing cesium methacrylate was more polar than this of ionomer containing cesium acrylate. Styrene-based ionomers containing 3.7 mol% of various alkali metal acrylates had less polar surfaces than initial copolymer and they were also more resistant to UV-irradiation in comparison to the initial copolymer. Copolymers obtained in emulsion and suitable ionomers had more polar surfaces and they were more sensitive to UV-light compared to copolymers obtained in bulk and their ionomers.

  17. Acrylic and Methacrylic Acids Obtaining by Gas-Phase Aldol Condensation of Carbonyl Compounds on B2O3?P2O5?WO3?V2O5/SiO2 Catalysts

    Nebesnyi, Roman; Petelka, Oksana; Shpyrka, Iryna

    2013-01-01

    Prospects of acrylic acid obtaining by acetic acid aldol condensation with formaldehyde are considered. Complex oxide catalysts of the process have been developed. It is shown that raw materials costs in case of acrylic acid production by the condensation method are commeasurable with those in case of its production by oxidation method (main industrial method of acrylic acid production).This method of acrylic acid obtaining may be used as an alternative and enables diversifying the raw materi...

  18. Synthesis and characterization of organometallic copolymers of acrylic acid g-polyethylene, with Mo, Fe, Co, Zn and Ni

    In this study, the preparation of a series of low density polyethylenes grafted with acrylic acid is presented. The grafting reactions were initiated by different doses of γ radiation; it was observed that grafting increased with the doses of radiation. The prepared copolymers were coordinated with different metals, as Mo, Fe, Co, Zn and Ni. The amount of metal supported on the polymer was determined by atomic absorption. Infrared spectroscopy and thermogravimetric analysis confirmed the metal chelation on the graft copolymer. The film surfaces were observed by scanning electron microscopy. positron annihilation spectroscopy revealed a decrease on the free volume in the low density polyethylene after the grafting with acrylic acid. (Author)

  19. The pH-responsive behaviour of poly(acrylic acid) in aqueous solution is dependent on molar mass.

    Swift, T; Swanson, L.; Geoghegan, M; Rimmer, S.

    2016-01-01

    Fluorescence spectroscopy on a series of aqueous solutions of poly(acrylic acid) containing a luminescent label showed that polymers with molar mass, Mn < 16.5 kDa did not exhibit a pH responsive conformational change, which is typical of higher molar mass poly(acrylic acid). Below this molar mass, polymers remained in an extended conformation, regardless of pH. Above this molar mass, a pH-dependent conformational change was observed. Diffusion-ordered nuclear magnetic resonance spectroscopy ...

  20. Poly (acrylic acid sodium) grafted carboxymethyl cellulose as a high performance polymer binder for silicon anode in lithium ion batteries

    Liangming Wei; Changxin Chen; Zhongyu Hou; Hao Wei

    2016-01-01

    The design of novel binder systems is required for the high capacity silicon (Si) anodes which usually undergo huge volume change during the charge/discharge cycling. Here, we introduce a poly (acrylic acid sodium)-grafted-carboxymethyl cellulose (NaPAA-g-CMC) copolymer as an excellent binder for Si anode in lithium ion batteries (LIBs). The NaPAA-g-CMC copolymer was prepared via a free radical graft polymerization method by using CMC and acrylic acid as precursors. Unlike the linear, one-dim...

  1. ABS polymer electroless plating through a one-step poly(acrylic acid) covalent grafting.

    Garcia, Alexandre; Berthelot, Thomas; Viel, Pascal; Mesnage, Alice; Jégou, Pascale; Nekelson, Fabien; Roussel, Sébastien; Palacin, Serge

    2010-04-01

    A new, efficient, palladium- and chromium-free process for the electroless plating of acrylonitrile-butadiene-styrene (ABS) polymers has been developed. The process is based on the ion-exchange properties of poly(acrylic acid) (PAA) chemically grafted onto ABS via a simple and one-step method that prevents using classical surface conditioning. Hence, ABS electroless plating can be obtained in three steps, namely: (i) the grafting of PAA onto ABS, (ii) the copper Cu(0) seeding of the ABS surface, and (iii) the nickel or copper metallization using commercial-like electroless plating bath. IR, XPS, and SEM were used to characterize each step of the process, and the Cu loading was quantified by atomic absorption spectroscopy. This process successfully compares with the commercial one based on chromic acid etching and palladium-based seed layer, because the final metallic layer showed excellent adhesion with the ABS substrate. PMID:20361751

  2. Use of acrylic acid in the synthesis of molecularly imprinted polymers for the analysis of cyproheptadine

    Feas, Xesus [Analytical Chemistry, Nutrition and Bromatology, Campus Lugo, University of Santiago de Compostela. E-27002, Lugo, Galiza (Spain); Fente, Cristina A. [Analytical Chemistry, Nutrition and Bromatology, Campus Lugo, University of Santiago de Compostela. E-27002, Lugo, Galiza (Spain)], E-mail: cfente@lugo.usc.es; Hosseini, S. Vali [Analytical Chemistry, Nutrition and Bromatology, Campus Lugo, University of Santiago de Compostela. E-27002, Lugo, Galiza (Spain); Seijas, Julio A. [Organic Chemistry, Campus Lugo, University of Santiago de Compostela. Aptdo 280, E-27080, Lugo (Spain); Vazquez, Beatriz I.; Franco, Carlos M.; Cepeda, Alberto [Analytical Chemistry, Nutrition and Bromatology, Campus Lugo, University of Santiago de Compostela. E-27002, Lugo, Galiza (Spain)

    2009-03-01

    The synthesis and comparative characterization of molecularly imprinted polymers (MIP{sub s}) with cyproheptadine (CYP), using two different monomers, acrylic acid (AA) and methacrylic acid (MAA), are described. Polyacids (PA) [poly(methacrylic acid) (PMAA) and poly(acrylic acid) (PAA)] were obtained by the radical polymerization of MAA and AA, respectively, in dichloromethane as the porogen solvent-imprinted medium. The non-covalent imprinting process was performed via thermal decomposition of an azo-initiator at 60 deg. C, using ethylene glycol dimethacrylate as the cross-linker and 2,2'-azobis(2-methylpropionitrile) as the initiator. The selectivities of MIP{sub s} and NIP{sub s} particles were evaluated in binding experiments of the four synthesized polymeric materials (MIP{sub aa}, MIP{sub maa}, NIP{sub maa} and NIP{sub aa}) with CYP. The effects of monomers on: a) the surface morphology, b) the binding capacity and c) the swelling properties of imprinted and non-imprinted polymers were studied and are presented here. Polymer material morphology was assessed with scanning electron microscopy (SEM). This revealed differences in monomer function, depending on which one was employed, as well as differences in function when polymerization occurred in the presence of template or without it. Non-specific retention of the template to NIP{sub s} was higher for NIP{sub s}-PAA polymers than for NIP{sub s}-PMAA materials. In terms of specific binding ({delta}Q = Q{sub MIP} - Q{sub NIP}), MIP{sub maa} showed the greatest value (53.47%) in comparison with MIP{sub aa} (50.07%)

  3. Electron-beam induced RAFT-graft polymerization of poly(acrylic acid) onto PVDF

    This paper explores for the first time the post-radiation-induced-graft polymerization on solid substrate using reversible addition-fragmentation transfer (RAFT) mechanism. Radiation-induced graft polymerization onto polymers is a potentially interesting technique to create easily new materials from highly resistant polymers, e.g. surface graft polymerization of acrylic acid (AA) onto poly(vinylidene difluoride) (PVDF) improves its surface properties without losing its excellent mechanical properties. As a consequence of the radical nature of the polymerization processes it is difficult to control molecular weight of grafted chains, and therefore design and standardize the properties of the final product. RAFT polymerization is a suitable method to obtain monodisperse polymers. The ability of the RAFT agents to control the polymer chain length could be an interesting approach to improve the grafted polymers obtained by post-radiation-induced-graft polymerization technique. In this way, graft polymerization of AA onto electron-beam irradiated α-PVDF was performed using trithiocarbonic acid bis(1-phenylethyl) ester as a RAFT agent to control the radical polymerization. We studied several grafting parameters such as solvent, monomer concentration and grafting time in order to achieve a poly(acrylic acid) (PAA) layer onto PVDF surface. Acetic acid was found to be the best solvent for many reasons, as to drive graft polymerization mainly to the polymer surface, complete solubility and stability of all reactants. Hydrolysis of PAA chains was also studied in order to remove the trithiocarbonate functionality from the grafted polymer. A mild chemical condition was achieved in order to have thiol groups that were detected onto the modified PVDF by specific enzymatic reaction

  4. Electron-beam induced RAFT-graft polymerization of poly(acrylic acid) onto PVDF

    Grasselli, M.; Betz, N.

    2005-07-01

    This paper explores for the first time the post-radiation-induced-graft polymerization on solid substrate using reversible addition-fragmentation transfer (RAFT) mechanism. Radiation-induced graft polymerization onto polymers is a potentially interesting technique to create easily new materials from highly resistant polymers, e.g. surface graft polymerization of acrylic acid (AA) onto poly(vinylidene difluoride) (PVDF) improves its surface properties without losing its excellent mechanical properties. As a consequence of the radical nature of the polymerization processes it is difficult to control molecular weight of grafted chains, and therefore design and standardize the properties of the final product. RAFT polymerization is a suitable method to obtain monodisperse polymers. The ability of the RAFT agents to control the polymer chain length could be an interesting approach to improve the grafted polymers obtained by post-radiation-induced-graft polymerization technique. In this way, graft polymerization of AA onto electron-beam irradiated α-PVDF was performed using trithiocarbonic acid bis(1-phenylethyl) ester as a RAFT agent to control the radical polymerization. We studied several grafting parameters such as solvent, monomer concentration and grafting time in order to achieve a poly(acrylic acid) (PAA) layer onto PVDF surface. Acetic acid was found to be the best solvent for many reasons, as to drive graft polymerization mainly to the polymer surface, complete solubility and stability of all reactants. Hydrolysis of PAA chains was also studied in order to remove the trithiocarbonate functionality from the grafted polymer. A mild chemical condition was achieved in order to have thiol groups that were detected onto the modified PVDF by specific enzymatic reaction.

  5. Decolourization performance in C. I. Vat Yellow 1 aqueous suspension using hydrophobically modified poly(acrylic acid).

    Chen, J; Chen, M C

    2011-01-01

    A series of hydrophobically modified poly(acrylic acid) (PAA), poly(2-phenoxyethyl acrylate-co-acrylic acid) (poly(PHEA-co-AA)), have been synthesized and characterized by Ubbelohde type viscometry, Nuclear Magnetic Resonance (1H NMR) spectrometry and Differential Scanning Calorimetry (DSC). The shear thinning Non-Newtonian fluid behavior of their aqueous solution and the dependence on pH and hydrophobic group contents were found through apparent viscosity and rheological property investigating. Decolourization performance in C. I. Vat Yellow 1 aqueous suspension was evaluated through visible absorbance data. Decolourization performance of hydrophobically associated polymer indicates two times better than that of PAA. The quantitative relationship was mainly studied. PMID:21866762

  6. UV-induced graft polymerization of acrylic acid in the sub-micronchannels of oxidized PET track-etched membrane

    Korolkov, Ilya V.; Mashentseva, Anastassiya A.; Güven, Olgun; Taltenov, Abzal A.

    2015-12-01

    In this article, we report on functionalization of track-etched membrane based on poly(ethylene terephthalate) (PET TeMs) oxidized by advanced oxidation systems and by grafting of acrylic acid using photochemical initiation technique for the purpose of increasing functionality thus expanding its practical application. Among advanced oxidation processes (H2O2/UV) system had been chosen to introduce maximum concentration of carboxylic acid groups. Benzophenone (BP) photo-initiator was first immobilized on the surfaces of cylindrical pores which were later filled with aq. acrylic acid solution. UV-irradiation from both sides of PET TeMs has led to the formation of grafted poly(acrylic acid) (PAA) chains inside the membrane sub-micronchannels. Effect of oxygen-rich surface of PET TeMs on BP adsorption and subsequent process of photo-induced graft polymerization of acrylic acid (AA) were studied by ESR. The surface of oxidized and AA grafted PET TeMs was characterized by UV-vis, ATR-FTIR, XPS spectroscopies and by SEM.

  7. Chelation in metal intoxication XXX: α-mercapto-β-aryl acrylic acids as antidotes to cadmium toxicity

    α-Mercapto-β-(2-furyl) acrylic acid (MFA), α-mercapto-β-(2-hydroxyphenyl) acrylic acid (MHA), β-1,2-phenylene di-α-mercaptoacrylic acid (1,2-PDMA) and β-l,4-phenylene di-α-mercapto acrylic acid (1,4-PDMA) were compared to sodium N-benzyl-D-glucamine dithiocarbamate (NBG-DTC) an effective cadmium chelator, for their ability to mobilize Cd and influence the Cd induced tissue metallothionein (MT) in rats administered 109CdCl2, 72 hr earlier. MFA was almost as effective as NBG-DTC but more effective than MHA in enhancing urinary and faecal excretion of Cd, reducing tissue and blood levels of Cd and in lowering Cd induced increase in hepatic and renal MT contents. 1,2-PDMA and l,4-PDMA were effective only in reducing the hepatic burden of Cd. The results do not indicate any direct relationship between the efficacy of α-mercapto-β-aryl acrylic acids to decorporate body Cd and their lipophilic-hydrophilic character or number-arrangement of their sulfhydryl groups. (author)

  8. Electromechanical reliability of flexible transparent electrodes during and after exposure to acrylic acid

    The effect of deposition temperature on pulsed laser deposition (PLD) fabricated flexible transparent electrodes subjected to mechanical loading, after exposure to acrylic acid, and the combined effect of fatigue and corrosion on sputter-deposited polyester-based indium tin oxide (ITO) films are both investigated in this study. Acrylic acid containing pressure sensitive adhesives, which are commonly used in various flexible device stacks, can corrode the ITO film. In addition, fatigue due to cyclic loading can lead to film cracking. The combined effect of fatigue and corrosion can lead to catastrophic failure of the system. We found that PLD-produced ITO on polyethylene naphthalate samples deposited at 150 °C performs better than samples deposited at 50 °C under uniaxial mechanical loading. They were found to exhibit higher crack onset strain than their 50 °C counterparts. However, they were observed to be more sensitive to increasing acid concentrations. Scanning electron microscopy images show a larger number of adhesive cracks on the surfaces of the 150 °C-deposited samples than the 50 °C-deposited samples. Atomic force microscopy results reveal that the increased temperature causes a significant increase in surface roughness which may affect the corrosion behavior of the ITO film. Furthermore, in situ electrical resistance measurements and crack density analysis suggest that the combination of fatigue and corrosion can cause film failure at low strains, less than those needed for failure with no corrosion. For example, at 0.9% applied strain and 500,000 cycles, the crack density under fatigue–corrosion is 1.7 times that of the fatigue-only case. - Highlights: ► ITO films were deposited on polymers with PLD or magnetron sputtering. ► The combination of fatigue and corrosion was investigated using a custom apparatus. ► Adhesion and film roughness played roles in the fatigue-corrosion behavior

  9. A new and direct synthesis of lactic acid from acrylic acid using an excimer laser with high intensity

    A new and direct method of XeF (351 nm) laser irradiation of acrylic acid 1 solution containing H2O2 are described for the chemical synthesis of lactic acid 2. Increase in the yield strongly depended on the irradiation dose and H2O2 feeding rate, and the formation of 2 showed the quantum yield, 0.3, and the selectivity, 50%, at the maximum yield. Product analysis indicated that OH radicals formed with high density by the laser-photolysis of H2O2 are equally bonded to the carbons of α- and β-positions of 1 to produce 2 and 3-hydroxy propanoic acid with ratio of 1 to 1. (author)

  10. A facile one pot strategy for the synthesis of well-defined polyacrylates from acrylic acid via RAFT polymerization.

    Li, Qianbiao; Wang, Taisheng; Dai, Jingwen; Ma, Chao; Jin, Bangkun; Bai, Ruke

    2014-03-28

    A facile one pot strategy for the preparation of linear and hyperbranched polyacrylates has been successfully developed by the combination of in situ esterification of acrylic acid with halogenated compounds promoted by 1,1,3,3-tetramethylguanidine (TMG) and RAFT polymerization. PMID:24534953

  11. Structure-function properties of amylose-oleic acid inclusion complexes grafted with poly(methyl acrylate)

    Spherulites, produced by steam jet-cooking high-amylose starch and oleic acid, were grafted with methyl acrylate, both before and after removal of un-complexed amylopectin. For comparison, granular high-amylose corn starch was graft polymerized in a similar manner. The amount of grafted and ungrafte...

  12. Comparison of various models to describe the charge-pH dependence of poly(acrylic acid)

    Lützenkirchen, J.; Male, van J.; Leermakers, F.A.M.; Sjöberg, S.

    2011-01-01

    The charge of poly(acrylic acid) (PAA) in dilute aqueous solutions depends on pH and ionic strength. We report new experimental data and test various models to describe the deprotonation of PAA in three different NaCl concentrations. A simple surface complexation approach is found to be very success

  13. Grafting of acrylic acid onto polypropylene films irradiated with argon ions

    Polypropylene (PP) foils were irradiated with 100 keV energy Argon ions at different fluences ranging from 1012 up to 2 x 1015 cm-2 and then grafted with acrylic acid (AA). The grafting yield was measured by weight difference and the structural changes on the films were analysed using Fourier transform infrared spectroscopy (FTIR). Different parameters that determined the grafting process such us fluence, grafting time and monomer concentration were analysed. The grafting reached an optimum value at 79% in aqueous solution at 30 min grafting time. The grafting yield as a function of the ion fluence plot, presented a maximum value, as previously found in a study of heavy beam on polymers

  14. Poly-Acrylic Acid Derivatives as Diesel Flow Improver for Paraffin-Based Daqing Diesel

    Cuiyu Jiang; Ming Xu; Xiaoli Xi; Panlun Qi; Hongyan Shang

    2006-01-01

    Since the diesel products from paraffin-based Daqing crude oil showed low sensitivity to certain commercial diesel pour point depressant (PPDs) that resulted from the high content of paraffin, certain poly-acrylic acid derivatives (PADE) with-COOR,-COOH,-CONHR, and -COO-NH3+R groups by molecular design on the mechanics of diesel; PPDs were synthesized and evaluated as cold flow improver for Daqing 0# diesel in this paper. The pure PADE was superior to the commercial PPDs and displayed a substantial ability of wax crystals dispersion. There was a synergistic effect among the PADE and T1804 and secondary amine. The synergism clearly improved the low temperature performance of Daqing diesel products and could reduce the cold filter plugging point of 0# diesel by 6-7 ℃.

  15. Michael-type addition of azoles of broad-scale acidity to methyl acrylate

    Krzysztof Z. Walczak

    2011-02-01

    Full Text Available An optimisation of Michael-type addition of azole derivatives of broad-scale acidity – ranging from 5.20 to 15.00 pKa units – namely 4-nitropyrazole, 3,5-dimethyl-4-nitropyrazole, 4(5-nitroimidazole, 4,5-diphenylimidazole, 4,5-dicyanoimidazole, 2-methyl-4(5-nitroimidazole, 5(4-bromo-2-methyl-4(5-nitroimidazole and 3-nitro-1,2,4-triazole to methyl acrylate as an acceptor was carried out. The optimisation process involved the use of an appropriate basic catalyst (DBU, DIPEA, NaOH, NaH, TEDA, a donor/base/acceptor ratio and the reaction temperature. The reactions were performed in DMF as solvent. Target Michael adducts were obtained in medium to excellent yields. Importantly, for imidazole and 1,2,4-triazole derivatives, no corresponding regioisomers were obtained.

  16. Adsorptive features of poli(acrylic acid-co-hydroxyapatite) composite for UO22+

    The copolymer of poli(acrylic acid-co-hydroxyapatite) (PAA-HAP) was prepared and characterized by means of FT-IR and SEM analysis. The adsorptive features of PAA-HAP for UO22+ was studied as a function of pH, adsorbent dosage, initial metal ion concentration and temperature. The adsorption isotherm data fitted well to the Langmuir isotherm model. The adsorbed UO22+ can be desorbed effectively by 0.1 M HNO3. The maximum adsorption capacities for UO22+ of the dry PAA-HAP was 1.86 x 10-4 mol/g. The high adsorption capacity and kinetics results indicate that PAA-HAP can be used as an alternative adsorbent to remove UO22+ from aqueous solution. (author)

  17. Cascade enzymatic catalysis in poly(acrylic acid) brushes-nanospherical silica for glucose detection.

    Zhao, Yan; Wang, Ying; Zhang, Xiaobin; Kong, Rongmei; Xia, Lian; Qu, Fengli

    2016-08-01

    The ultrasensitive monitoring of glucose with a fast and accurate method is significant in potential therapeutics and optimizes protein biosynthesis. Incorporation of enzyme into matrix is considered as promising candidates for constructing highly sensitive glucose-responsive systems. In this study, three-dimensional poly(acrylic acid) brushes-nanospherical silica (PAA-nano silica) with high amplification capability and stability were used to covalently immobilize bienzymes for cascade enzymatic catalysis. The major advantages of PAA-nano silica-bienzyme co-incorporation is that the enzymes are proximity distribution, and such close confinement both minimized the diffusion of intermediates among the enzymes in the consecutive reaction and improve the utilization efficiency of enzymes, thereby enhancing the overall reaction efficiency and specificity. Thus, this present bienzymatic biosensor shows robust signal amplification and ultrasensitivity of glucose-responsive properties with a detection limit of 0.04μM. PMID:27216683

  18. Study on swelling behaviour of hydrogel based on acrylic acid and pectin from dragon fruit

    Abdullah, Mohd Fadzlanor; Lazim, Azwani Mat

    2014-09-01

    Biocompatible hydrogel based on acrylic acid (AA) and pectin was synthesized using gamma irradiation technique. AA was grafted onto pectin backbone that was extracted from dragon fruit under pH 3.5 and extracts and ethanol ratios (ER) 1:0.5. The optimum hydrogel system with high swelling capacity was obtained by varying the dose of radiation and ratio of pectin:AA. FTIR-ATR spectroscopy was used to verify the interaction while thermal properties were analyzed by TGA and DSC. Swelling studies was carried out in aqueous solutions with different pH values as to determine the pH sensitivity. The results show that the hydrogel with a ratio of 2:3 (pectin:AA) and 30 kGy radiation dose has the highest swelling properties at pH of 10.

  19. Dielectric properties of solution-grown-undoped and acrylic-acid-doped ethyl cellulose

    P K Khare; Sandeep K Jain

    2000-02-01

    Dielectric capacities and losses were measured, in the temperature (50–170°C) and frequency (01–100 kHz range), for undoped and acrylic acid (AA) doped ethyl cellulose (EC) films (thickness about 20 m) with progressive increase in the concentration of dopant in the polymer matrix. The variation of capacity with temperature is attributed to thermal expansion in the lower temperature region to the orientation of dipolar molecules in the neighbourhood of glass transition temperature () and random thermal motion of molecules above . The dielectric losses exhibit a broad peak. Doping with AA is found to affect the magnitude and position of the peak. AA is found to have a two-fold action. Firstly, it enhances the chain mobility and secondly, it increases the dielectric loss by forming charge transfer complexes.

  20. Superabsorbent Prepared by Radiation Induced Graft Copolymerization of Acrylic Acid onto Cassava Starch. Chapter 18

    Superabsorbent was synthesized by radiation induced graft polymerization of acrylic acid onto cassava starch. Parameters such as the absorbed dose and the amount of monomer were investigated in order to determine the optimum conditions for the grafting polymerization. Water retention, germination percentage, and germination energy were also determined in order to evaluate the possibility of superabsorbent in agricultural applications, especially in arid regions. The graft copolymer was characterized by the Fourier transform infrared spectroscopy (FTIR). Results indicated that the sand mixed with 0.1% wt superabsorbent could absorb more water than the sand without superabsorbent. The germination energy of corn seeds mixed with 0.5% superabsorbent was obviously higher than those without superabsorbent. These experimental results showed that the superabsorbent has considerable effects on seed germination and the growth of young plants. (author)

  1. Property and AFM analysis of copolymer from konjac graft acrylic acid by irradiation

    The water absorption property and construction of konjac glucomannon, copolymer and regenerated copolymer demonstrated by Atomic Force Microscopy(AFM)was studied in this paper. Result showed that the copolymer was 887.8 times distilled water and the water absorption of konjac glucomannan was only 60 times. The biggest water absorption speed of distilled water was 64.7 g.g-1. min-1.The water reserving percent was 92% at room temperature after 24 h from fully water absorbing.The largest second tap water absorption was 366 times which was higher than the first. The AFM images indicated konjac grafts acrylic acid and hydrophilic sturcture comes into being. During the course of regeneration the dimensional sturcture of the copolymer was changed to more regularly.So the water absorption of copolymer was higher than konjac and regenerater's was higher than copolymer. (authors)

  2. Poly(acrylic acid)-stabilized colloidal gold nanoparticles: synthesis and properties

    Combining the intriguing optical properties of gold nanoparticles with the inherent physical and dynamic properties of polymers can give rise to interesting hybrid nanomaterials. In this study, we report the synthesis of poly(acrylic acid) (PAA)-capped gold nanoparticles. The polyelectrolyte-wrapped gold nanoparticles were fully characterized and studied via a combination of techniques, i.e. UV-vis and infrared spectroscopy, dark field optical microscopy, SEM imaging, dynamic light scattering and zeta potential measurements. Although PAA-capped nanoparticles have been previously reported, this study revealed some interesting aspects of the colloidal stability and morphological change of the polymer coating on the nanoparticle surface in an electrolytic environment, at various pH values and at different temperatures.

  3. Thermal degradation of biopolymer binders: the example of starch-poly(acrylic acid

    B. Grabowska

    2010-01-01

    Full Text Available To characterise a polymer, it is of fundamental importance to determine its parameters, like the temperatures of destruction, vitrification, melting point, specific mass losses or polymorphic transformations, which frequently determine the quality of the product and its applications. Thermal analyses were conducted of samples of a biopolymer binder: a starch-poly(acrylic acid composition and a moulding sand with a biopolymer binder previously hardened with microwaves. In order to determine the thermal stability of the examined samples by determining the destruction temperature and the thermal effects of transformations taking place during heating, FTIR spectroscopy and thermal analysis (DSC, DTG, TG methods were used. In addition, volatile products of degradation were analysed using the thermogravimetry (TG method coupled online with mass spectrometry (MS. These examinations were also aimed at identifying the changes that can take place in the moulding sand when it comes into contact with liquid metal.

  4. Grafting of acrylic acid on etched latent tracks induced by swift heavy ions on polypropylene films

    In order to continue with a systematic study that include different polymers and monomers, the residual active sites produced by heavy ion beams, that remain after the etching process, were used to start the grafting process. To produce tracks, foils of polypropylene (PP) were irradiated with 208Pb of 25.62 MeV/n. Then, these were etched and grafted with acrylic acid (AA) monomers. Experimental curves of grafting yield as a function of grafting time with the etching time as a parameter were measured. Also, the grating yield as a function of the fluence and etching time was obtained. In addition, the permeation of solutions, with different pH, through PP grafted foils was measured

  5. Preparation of porous chitosan-poly(acrylic acid)-calcium phosphate hybrid nanoparticles via mineralization

    CHEN ChangJing; DENG Yu; YAN ErYun; HU Yong; JIANG XiQun

    2009-01-01

    In this work,the preparation of chitosan-poly(acrylic acid)-calcium phosphate hybrid nanoparticles (CS-PAA-CaP NP) based on the mineralization of calcium phosphate (CAP) on the surface of chitosan-poly (acrylic acid) nanoparticles (CS-PAA NPs) was reported. CS-PAA-CaP NPs were achieved by directly adding ammonia to the aqueous solution of CS-PAA nanoparticles or by thermal decomposition of urea in the aqueous solution of CS-PAA nanoparticles,resulting in the mineralization of CaP on the surface of CS-PAA NPs. Through these two routes,especially using urea as a pH-regulator,the precipitation of CS-PAA NPs,a common occurrence in basic environment,was avoided. The size,morphology and ingredient of CS-PAA-CaP hybrid nanoparticles were characterized by dynamic light scattering (DLS),transmission electron microscope (TEM),scanning electron microscope (SEM),thermogravimetry analysis (TGA) and X-ray diffractometer (XRD). When urea was used as the pH regulator to facilitate the mineralization during the thermal urea decomposition procedure,regular CS-PAA-CaP hybrid nanoparticles with a porosity-structural CaP shells and 400-600 nm size were obtained. TGA result revealed that the hybrid NPs contained approximately 23% inorganic component,which was consistent with the ratio of starting materials. The XRD spectra of hybrid nanoparticles indicated that dicalcium phosphate (DCP:CaHPO4) crystal was a dominant component of mineralization.The porous structure of the CS-PAA-CaP hybrid NPs might be greatly useful in pharmaceutical and other medical applications.

  6. Fluorescence and Judd-Ofelt analysis of rare earth complexes with maleic anhydride and acrylic acid

    WEN Shipeng; ZHANG Xiaoping; HU Shui; ZHANG Liqun; LIU Li

    2008-01-01

    Two kinds of Eu-complexes, Eu(TTA)2(Phen)(AA) and Eu(TTA)2(Phen)(MA) (HTFA=2-Thenoyltrifluoroacetone, Phen=1,10-phenanthroline, AA=acrylic acid, MA=Maleic anhydride), which combined the excellent fluorescence properties of Eu(TTA)2(Phen)(H2O) and the reactivity of acrylic acid and maleic anhydride with radicals, were synthesized. The two complexes were characterized by elemental analysis, infrared (IR) spectra, and X-ray photoelectron spectroscopy (XPS). Based on the data shown from the fluorescent spectra of the Eu-MA and Eu-AA complexes, the Ωλ (λ=2 and 4) experimental intensity parameters were calculated. The results demonstrated that the Ω2 intensity parameters for the two complexes were smaller than those for the Eu(TTA)2(Phen)(H2O) complex, indicating that a less symmetri-cal chemical environment existed in the complexes. It implied that the radiative efficiency of the 5D0 of these two complexes could be en-hanced by ligand of MA and AA, respectively. The luminescent lifetime of the Eu-AA (τ=7.26×10-4 s) or Eu-MA complex (τ=-8.12×10-4 s) was higher than that of the Eu(TTA)2(Phen)(H2O) complex, which was attributed to the substitution of the water molecule (H2O) in Eu(TTA)2(Phen)(H2O) by the MA or AA ligand.

  7. Corrosion Inhibitive Evaluation of an Environmentally Friendly Water-Base Acrylic Terpolymer on Mild Steel in Hydrochloric Acid Media

    Azghandi, Mojtaba Vakili; Davoodi, Ali; Farzi, Gholam Ali; Kosari, Ali

    2013-12-01

    The corrosion inhibitive performance of an environmentally friendly water-base acrylic terpolymer [methyl methacrylate/Butyl Acrylate/Acrylic acid (ATP)] on mild steel in 1 M HCl was investigated by alternating current and direct current electrochemical techniques and the quantum chemical method. An efficiency of more than 97 pct was obtained with 0.8 mmol/L ATP. The increase in inhibitor concentration and immersion time has a positive effect, while the temperature influence is negligible on the inhibitor efficiency. The present terpolymer obeys the Langmuir isotherm, and thermodynamic calculation reveals a chemisorption type on the surface. Density functional calculations showed that the lone pairs of electrons of oxygen in the structure of three monomers are suitable sites to adsorb onto the metal surface. Finally, in the presence of ATP, a decrease in surface roughness and corrosion attacks was demonstrated by atomic force microscopy and optical microscopy examinations, respectively.

  8. Thiomers: Influence of molecular mass and thiol group content of poly(acrylic acid) on efflux pump inhibition.

    Grabovac, Vjera; Laffleur, Flavia; Bernkop-Schnürch, Andreas

    2015-09-30

    The aim of the present study was to investigate the influence of molecular mass and thiol group content of poly(acrylic acid)-cysteine conjugates on the permeation of sulforhodamine 101 and penicillin G. acting as substrates for multidrug resistance-associated protein 2 efflux pump. Poly(acrylic acids) of 2 kDa, 100 kDa, 250 kDa, 450 kDa and 3000 kDa were conjugated with cysteine. The thiol group content of all these polymers was in the range from 343.3 ± 48.4 μmol/g to 450.3 ± 76.1 μmol/g. Transport studies were performed on rat small intestine mounted in Ussing-type chambers. Since 250 kDa poly(acrylic acid) showed the highest permeation enhancing effect, additionally thiolated 250 kDa polyacrylates displaying 157.2 μmol/g, 223.0 ± 18.1 and 355.9 μmol/g thiol groups were synthesized in order to investigate the influence of thiol group content on the permeation enhancement. The permeation of sulforhodamine was 3.93- and 3.85-fold improved using 250 kDa poly(acrylic acid)-cysteine conjugate exhibiting 355.9 ± 39.5 μmol/g and 223.0 ± 18.1 μmol/g thiol groups. Using the same conjugates the permeation of penicillin G was 1.70- and 1.59-fold improved, respectively. The study demonstrates that thiolated poly(acrylic acid) inhibits Mrp2 mediated transport and that the extent of inhibition depends on the molecular mass and degree of thiolation of the polymer. PMID:26238816

  9. pH-Responsive Behavior of Poly(acrylic acid) Brushes of Varying Thickness

    Yadav, Vivek; Robertson, Megan; Conrad, Jacinta

    2015-03-01

    We have investigated the pH-dependent response of polyelectrolyte brushes of varying thickness. Our model system consists of poly(acrylic acid) brushes, which change from hydrophobic and neutral at low pH to hydrophilic and negatively charged at high pH, synthesized using a grafting-from approach at constant grafting density. As the polymer brush thickness increased, the brushes exhibited greater hysteresis in static water contact angle as a function of pH. We extracted the pKa of the polymer brushes from contact angle measurements. The relationship between the pKa and brush thickness depended on the order in which the brushes were exposed to solutions of varying pH: pKa decreased on increasing brush thickness when going from basic to acidic medium whereas pKa increased on increasing brush thickness when going from acidic to basic medium. We speculate that the origin of hysteresis can be explained by pH-dependent conformational changes in these polyelectrolyte brushes.

  10. Controlled release of insulin through hydrogels of (acrylic acid)/trimethylolpropane triacrylate

    Raymundi, Vanessa C.; Aguiar, Leandro G.; Souza, Esmar F.; Sato, Ana C.; Giudici, Reinaldo

    2015-12-01

    Hydrogels of poly(acrylic acid) crosslinked with trimethylolpropane triacrylate (TMPTA) were produced through solution polymerization. After these hydrogels were loaded with insulin solution, they evidenced swelling. Experiments of controlled release of insulin through the hydrogels were performed in acidic and basic media in order to evaluate the rates of release of this protein provided by the referred copolymer. Additionally, a mathematical description of the system based on differential mass balance was made and simulated in MATLAB. The model consists of a system of differential equations which was solved numerically. As expected, the values of swelling index at the equilibrium and the rates of insulin release were inversely proportional to the degree of crosslinking. The mathematical model provided reliable predictions of release profiles with fitted values of diffusivity of insulin through the hydrogels in the range of 6.0 × 10-7-1.3 × 10-6 cm2/s. The fitted and experimental values of partition coefficients of insulin between the hydrogel and the medium were lower for basic media, pointing out good affinity of insulin for these media in comparison to the acidic solutions.

  11. Synthesis of poly acrylic acid modified silver nanoparticles and their antimicrobial activities

    Ni, Zhihui [Key Laboratory for Special Functional Materials of Ministry of Education, Henan University, Kaifeng 475004 (China); Wang, Zhihua [Institute of Environmental and Analytical Sciences, College of Chemistry and Chemical Engineering, Henan University, Kaifeng 475004 (China); Sun, Lei, E-mail: sunlei@henu.edu.cn [Key Laboratory for Special Functional Materials of Ministry of Education, Henan University, Kaifeng 475004 (China); Li, Binjie [Key Laboratory of Cellular and Molecular Immunology, Henan University, Kaifeng 475004 (China); Zhao, Yanbao [Key Laboratory for Special Functional Materials of Ministry of Education, Henan University, Kaifeng 475004 (China)

    2014-08-01

    Poly acrylic acid modified silver (Ag/PAA) nanoparticles (NPs) have been successfully synthesized in the aqueous solution by using tannic acid as a reductant. The structure, morphology and composition of Ag/PAA NPs were characterized by various techniques such as X-ray powder diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible absorption spectroscopy (UV–vis) and thermogravimetry analysis (TGA). The results show that PAA/Ag NPs have a quasi-ball shape with an average diameter of 10 nm and exhibit well crystalline, and the reaction conditions have some effect on products morphology and size distribution. In addition, the as-synthesized Ag/PAA NPs antimicrobial activities against Escherichia coli (E. coli), Pseudomonas aeruginosa (P. aeruginosa) and Staphylococcus aureus (S. aureus) were evaluated by the methods of broth dilution, cup diffusion, optical density (OD600) and electron microscopy observation. The as-synthesized Ag/PAA NPs exhibit excellent antibacterial activity. The antimicrobial mechanism may be attributed to the damaging of bacterial cell membrane and causing leakage of cytoplasm. - Highlights: • Dispersed Ag/PAA NPs with small size were synthesized. • Ag/PAA NPs exhibited excellent antimicrobial properties. • Interaction mechanism between Ag/PAA NPs and bacteria was verified.

  12. Synthesis of poly acrylic acid modified silver nanoparticles and their antimicrobial activities

    Poly acrylic acid modified silver (Ag/PAA) nanoparticles (NPs) have been successfully synthesized in the aqueous solution by using tannic acid as a reductant. The structure, morphology and composition of Ag/PAA NPs were characterized by various techniques such as X-ray powder diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible absorption spectroscopy (UV–vis) and thermogravimetry analysis (TGA). The results show that PAA/Ag NPs have a quasi-ball shape with an average diameter of 10 nm and exhibit well crystalline, and the reaction conditions have some effect on products morphology and size distribution. In addition, the as-synthesized Ag/PAA NPs antimicrobial activities against Escherichia coli (E. coli), Pseudomonas aeruginosa (P. aeruginosa) and Staphylococcus aureus (S. aureus) were evaluated by the methods of broth dilution, cup diffusion, optical density (OD600) and electron microscopy observation. The as-synthesized Ag/PAA NPs exhibit excellent antibacterial activity. The antimicrobial mechanism may be attributed to the damaging of bacterial cell membrane and causing leakage of cytoplasm. - Highlights: • Dispersed Ag/PAA NPs with small size were synthesized. • Ag/PAA NPs exhibited excellent antimicrobial properties. • Interaction mechanism between Ag/PAA NPs and bacteria was verified

  13. Synthesis of poly(acrylic acid-maleic acid)SiO2/Al2O3 as novel composite material for cesium removal from acidic solutions

    A novel composite material of SiO2-Al2O3 based on poly(acrylic acid-maleic acid) was synthesized by irradiated with 60Co γ-rays at a dose of 25 KGy. The composite material was characterized using FTIR, TGA and BET surface area. Adsorption of 134Cs from HNO3 was studied as a function of contact time, temperature and concentration of Cs. Sorption behavior of 134Cs in different concentration of HCl, HNO3, acetic acid, ascorbic acid, citric acid, NaCl and NaNO3 solutions has been investigated. It can be concluded that the P(AA-MA)/SiO2/Al2O3 is promising adsorbent for Cs removal from acidic liquid radioactive waste. (author)

  14. The effect of unsaturated fatty acid and triglyceride oil addition on the mechanical and antibacterial properties of acrylic bone cements.

    Persson, Cecilia; Robert, Elise; Carlsson, Elin; Robo, Céline; López, Alejandro; Godoy-Gallardo, Maria; Ginebra, Maria-Pau; Engqvist, Håkan

    2015-09-01

    Acrylic bone cements have an elastic modulus several times higher than the surrounding trabecular bone. This has been hypothesized to contribute to certain clinical complications. There are indications that the addition of specific fatty acids and triglyceride oils may reduce the elastic modulus of these types of cements. Some of these additives also appear to have inherent antibiotic properties, although this has never been evaluated in bone cements. In this study, several types of fatty acids and triglyceride oils were evaluated for use in acrylic bone cements. Their mechanical properties were evaluated under uniaxial compression testing and selected cements were then further characterized in terms of microstructure, handling and antibacterial properties using scanning electron microscopy, polymerization temperature measurements, agar diffusion tests and bactericidal activity assays of cement extracts. It was found that any of the evaluated fatty acids or triglyceride oils could be used to tailor the stiffness of acrylic bone cements, although at varying concentrations, which also depended on the type of commercial base cement used. In particular, the addition of very small amounts of linoleic acid (agar diffusion test as well as demonstrating 100% bactericidal activity against the same strain. PMID:25876889

  15. Preparation, characterization, and antibacterial activity studies of silver-loaded poly(styrene-co-acrylic acid) nanocomposites.

    Song, Cunfeng; Chang, Ying; Cheng, Ling; Xu, Yiting; Chen, Xiaoling; Zhang, Long; Zhong, Lina; Dai, Lizong

    2014-03-01

    A simple method for preparing a new type of stable antibacterial agent was presented. Monodisperse poly(styrene-co-acrylic acid) (PSA) nanospheres, serving as matrices, were synthesized via soap-free emulsion polymerization. Field-emission scanning electron microscopy micrographs indicated that PSA nanospheres have interesting surface microstructures and well-controlled particle size distributions. Silver-loaded poly(styrene-co-acrylic acid) (PSA/Ag-NPs) nanocomposites were prepared in situ through interfacial reduction of silver nitrate with sodium borohydride, and further characterized by transmission electron microscopy and X-ray diffraction. Their effects on antibacterial activity including inhibition zone, minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and bactericidal kinetics were evaluated. In the tests, PSA/Ag-NPs nanocomposites showed excellent antibacterial activity against both gram-positive Staphylococcus aureus and gram-negative Escherichia coli. These nanocomposites are considered to have potential application in antibacterial coatings on biomedical devices to reduce nosocomial infection rates. PMID:24433897

  16. Electron Beam Synthesis and Characterization of Acrylamide/Acrylic Acid Hydrogels Using Trimethylolpropane Trimethacrylate as Cross-Linker

    Gabriela Craciun

    2016-01-01

    Full Text Available The purpose of the paper is to present the synthesis and characterization of hydrogels prepared by free-radical copolymerization of acrylamide and acrylic acid in aqueous solutions using potassium persulfate as initiator and trimethylolpropane trimethacrylate as cross-linker, via the radiation technique. The samples were subjected to electron beam treatment in the dose range of 2 to 4 kGy and the influence of the absorbed dose and amount of cross-linker on the swelling properties, diffusion coefficient, and network parameters of hydrogels was investigated. A possible reaction mechanism for acrylamide/acrylic acid/trimethylolpropane trimethacrylate hydrogels was also suggested. The structure and morphology of hydrogels were characterized by Fourier Transform Infrared Spectroscopy and Scanning Electron Microscopy.

  17. Synthesis of Hydrogel Based on Nata De Coco and Acrylic Acid as Co-Monomer Using Free Radical Polymerization Method

    Nata de Coco or known as bacterial cellulose is produced by Acetobacter xylinum where it is more stable than plant cellulose. Moreover, it also provides outstanding advantages to be developed as an environmental responsive hydrogels. In this study the bacterial cellulose-g-acrylic acid hydrogel was synthesized by using a free radical polymerization method. Ammonium persulfate (APS) was used to initiate the reaction, while N,N'-methylene bis acrylamide has been used as the crosslinking agent. In order to test the hydrogel respond, swelling tests were made at different pH. Furthermore, ATR-FTIR analysis was used to determine the interactions between bacterial cellulose and acrylic acid. Finally, the determination of glass transition (Tg) was made by using DSC. (author)

  18. The influence of poly(acrylic) acid number average molecular weight and concentration in solution on the compressive fracture strength and modulus of a glass-ionomer restorative.

    Dowling, Adam H

    2011-06-01

    The aim was to investigate the influence of number average molecular weight and concentration of the poly(acrylic) acid (PAA) liquid constituent of a GI restorative on the compressive fracture strength (σ) and modulus (E).

  19. Rapid 3D Patterning of Poly(acrylic acid) Ionic Hydrogel for Miniature pH Sensors.

    Yin, Ming-Jie; Yao, Mian; Gao, Shaorui; Zhang, A Ping; Tam, Hwa-Yaw; Wai, Ping-Kong A

    2016-02-17

    Poly(acrylic acid) (PAA), as a highly ionic conductive hydrogel, can reversibly swell/deswell according to the surrounding pH conditions. An optical maskless -stereolithography technology is presented to rapidly 3D pattern PAA for device fabrication. A highly sensitive miniature pH sensor is demonstrated by in situ printing of periodic PAA micropads on a tapered optical microfiber. PMID:26643765

  20. Improvement in the behavior of bromelain coupled to pNIPAm polymers containing acrylamide or acrylic acid

    Rubab Mahmood

    2014-01-01

    Bromelain was coupled to N-isopropyl acrylamide (NIPAm)polymers, synthesized using NIPAm and various concentrations of acrylamide (Ac) or acrylic acid (AAc). Incorporation of Ac/AAcinto the polymer increased the LCST (lower critical solutiontemperature) in a concentration dependent manner but AAc wasmore effective in this regard; the LCST rose to 40°C when 6 percent AAc was used. Incorporation of Ac/AAc increased the coupling of enzyme to the polymer and the η (effectiveness factor) o...

  1. Structural Parameters and Swelling Behavior of pH Sensitive Poly(acrylamide-co-acrylic acid) Hydrogels

    Thakur, A; Wanchoo, R. K.; Singh, P

    2011-01-01

    In the present work, hydrogels based on acrylamide (AAm) and acrylic acid (AAc), crosslinked with N,N’-methylenebisacrylamide (MBAAm) were prepared by free radical polymerization in solution. The effect of initial AAm/AAc mole ratio and nominal crosslinking ratio (moles of crosslinking agent/moles of polymer repeat unit) on the dynamic and equilibrium swelling behaviour of hydrogels was investigated. Hydrogels were characterized by the polymer volume fraction in the swollen state (ν2,s ), the...

  2. Poly(acrylic acid) interpolymer complexation: use of a fluorescence time resolved anisotropy as a poly(acrylamide) probe

    Swift, T.; Swanson, L; Rimmer, S.

    2014-01-01

    A low concentration poly(acrylamide) sensor has been developed which uses the segmental mobility of another polymer probe with a covalently attached fluorescent marker. Interpolymer complexation with poly(acrylic acid) leads to reduced segmental mobility which can be used to determine the concentration of polymer in solution. This technique could be useful in detecting the runoff of polymer dispersants and flocculants in fresh water supplies following water purification processes

  3. Experimental Study and Numerical Solution of Poly Acrylic Acid Supported Magnetite Nanoparticles Transport in a One-Dimensional Porous Media

    M. Golzar; S. F. Saghravani; Azhdari Moghaddam, M.

    2014-01-01

    Recently, iron nanoparticles have attracted more attention for groundwater remediation due to its potential to reduce subsurface contaminants such as PCBs, chlorinated solvents, and heavy metals. The magnetic properties of iron nanoparticles cause to attach to each other and form bigger colloid particles of iron nanoparticles with more rapid sedimentation rate in aqueous environment. Using the surfactants such as poly acrylic acid (PAA) prevents iron nanoparticles from forming large flocs tha...

  4. Obtention and characterization of acrylic acid-i-polyethylene organometallic copolymers with Mo, Fe, Co, Zn, and Ni

    In this study a graft acrylic acid (AA) in low density polyethylene (PEBD) copolymers were prepared, using as reaction initiator, gamma radiation at different doses. These copolymers were coordinated with molybdenum, cobalt, iron, zinc and nickel. the obtained polymeric materials were characterized by conventional analysis techniques. It was studied the measurement parameter variation of the positron annihilation when they inter activated with this type of materials and so obtaining information about microstructure of these polymers. (Author)

  5. Synthesis and characterization of polycaprolactone/acrylic acid (PCL/AA) hydrogel for controlled drug delivery

    Nazar Mohammad Ranjha; Jahanzeb Mudassir; Sajid Majeed

    2011-12-01

    In the present work biodegradable pH-sensitive polycaprolactone/acrylic acid (PCL/AA) hydrogels have been developed using ethylene glycol dimethacrylate (EGDMA) as a cross-linker and benzoyl peroxide as initiator. For these prepared hydrogels swelling studies, sol–gel fraction analysis and porosity measurements were performed. Results show that swelling of the hydrogels decreases on increasing the concentration of PCL and EGDMA, however swelling of hydrogels increases on increasing the concentration of AA. Results of sol–gel fraction analysis show that gel fraction increases on increasing concentration of monomer AA, polymer PCL as well as cross-linker EGDMA. As far as porosity is concerned, it increases on increasing the concentration of AA and PCL while porosity decreases on increasing the concentration of EGDMA. Hydrogels were characterized by measuring diffusion coefficient () and equilibrium water content (EWC). Network formation, morphology and crystallinity of PCL/AA hydrogels were investigated using FTIR, SEM and XRD, respectively. Tramadol hydrochloride was loaded as model drug and its release pattern was analysed using various kinetic models like zero order, first order, Higuchi and Peppas. Results indicated that most of the samples followed non-Fickian release mechanism.

  6. Studies on surface graft polymerization of acrylic acid onto PTFE film by remote argon plasma initiation

    The graft polymerization of acrylic acid (AAc) was carried out onto poly(tetrafluoroethylene) (PTFE) films that had been pretreated with remote argon plasma and subsequently exposed to oxygen to create peroxides. Peroxides are known to be the species responsible for initiating the graft polymerization when PTFE reacts with AAc. We chose different parameters of remote plasma treatment to get the optimum condition for introducing maximum peroxides (2.87 x 10-11 mol/cm2) on the surface. The influence of grafted reaction conditions on the grafting degree was investigated. The maximum grafting degree was 25.2 μg/cm2. The surface microstructures and compositions of the AAc grafted PTFE film were characterized with the water contact angle meter, Fourier-transform infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS). Contact angle measurements revealed that the water contact angle decreased from 108o to 41o and the surface free energy increased from 22.1 x 10-5 to 62.1 x 10-5 N cm-1 by the grafting of the AAc chains. The hydrophilicity of the PTFE film surface was greatly enhanced. The time-dependent activity of the grafted surface was better than that of the plasma treated film

  7. Thermal Properties of Poly(allylamine hydrochloride)/Poly(acrylic acid) Layer-by-Layer Assemblies

    Lutkenhaus, Jodie; Shao, Lin

    2010-03-01

    Layer-by-layer (LbL) assemblies are promising for global energy and health applications, but their materials properties are not well understood. LbL assemblies are created from the alternate adsorption of oppositely charged species from solution to a substrate. Particularly, little is known about the thermal properties of LbL assemblies because the supporting substrate impedes characterization. It is not initially clear if electrostatic LbL assemblies possess a glass transition temperature, if they are rubbery or glassy, or if their heat capacity is comparable to their homopolymer constituents. Here, we isolate large areas of LbL assemblies from a low-energy substrate, which facilitates thermal characterization via modulated differential scanning calorimetry (MDSC) and thermal gravimetric analysis (TGA). LbL assemblies of poly(acrylic acid) (PAA) and poly(allylamine hydrochloride) (PAH) were deposited onto hydrophobic substrates, and subsequently isolated. Results highlight that PAH/PAA LbL films are glassy, and have low mobility because of the high density of ion pair crosslinks. The techniques presented here are general, and can be applied to any LbL film.

  8. Radiation grafting of ionically crosslinked alginate/chitosan beads with acrylic acid for lead sorption

    Radiation-induced grafting of acrylic acid onto alginate/chitosan beads was performed in solution at a dose rate of 20.6 Gy/min of Co-60 gamma rays. The effect of absorbed dose on grafting yield was investigated. The characterization of the grafted and un-grafted beads was performed by FTIR spectroscopy and the swelling measurements at different pHs was studied. It is found that as the pH value increases the swelling degree increases up to pH 6 but with further increase in pH value the swelling decreases. Also, it is noticed that the grafting yield increased with increase the irradiation dose. Both un-grafted and grafted alginate/chitosan beads were examined as sorbents for the removal of Pb ions from aqueous solutions. The sorption behavior of the sorbents was examined through pH, and equilibrium measurements. Grafted alginate/chitosan beads presented higher sorption capacity for Pb ions than un-grafted beads. (author)

  9. Synthesis, structure and phase transition property of acrylic acid grafted paraffin

    Zhao, Xiaowen; Liu, Pengfei; Ye, Lin

    2014-05-01

    Polar monomer acrylic acid (AA) was used to modify paraffin in order to improve the latent heat of paraffin as phase change materials. The composition and sequence structure of the grafted products were characterized by FTIR, 13C NMR, 1H NMR and GPC analysis, and the thermal properties of paraffin-g-AA were investigated. It was found that AA was confirmed to be grafted onto the molecular chain of paraffin successfully. The mechanism of free radical grafting of AA may be only monomeric grafts. At low grafting ratio, the structure B can be mainly formed as a result of the radical coupling termination; while at the high grafting ratio, structure A was the primary structure as a result of the radical chain growth process. The number-average molecular weight of the grafted samples increased at first but leveled off with increasing grafting ratio, while the weight-average molecular weight increased gradually. The latent heat capacity of the grafted paraffin can be improved obviously at low grafting ratio due to the formation of structure B.

  10. Study on Radiated Polymerization of Acrylic Acid on Montmorillonite and Bentonite Used as Bioactivity Carriers

    The radiated polymerization of acrylic acid (AAc) on bentonite (BT) and montmorillonite (MMT) having structured silicate layers to produce hybrid materials were investigated. AAc concentrations of 10 and 40 % w/w were used to polymerize with MMT and BT at the absorbed doses of 3.6 and 6.4 kGy, respectively. The formed PAAc concentration of MMT-PAAc was 68 % and 40 % for BT-PAAc. The results of X-ray diffraction patterns were indicated that, the basal distances (d001) of MMT and BT after polymerization were ≈ 15 Å compared with BT was 12.17 Å and MMT did not appear the d001 peak. The cellulase immobilized yields of MMT-AAc and BT-AAc were determined by Lowry method with values were of 40.6 % and 68.3 %, respectively. The cellulase activity of the immobilization samples were checked by diffusion the sample solutions on agar after that measure of diameter of CMC hydrolysis circles. The results indicated that, the immobilized cellulase samples still maintain enzymatic activity after three times reuse. (author)

  11. Mechanically stable thermally crosslinked poly(acrylic acid)/reduced graphene oxide aerogels.

    Ha, Heonjoo; Shanmuganathan, Kadhiravan; Ellison, Christopher J

    2015-03-25

    Graphene oxide (GO) aerogels, high porosity (>99%) low density (∼3-10 mg cm(-3)) porous materials with GO pore walls, are particularly attractive due to their lightweight, high surface area, and potential use in environmental remediation, superhydrophobic and superoleophilic materials, energy storage, etc. However, pure GO aerogels are generally weak and delicate which complicates their handling and potentially limits their commercial implementation. The focus of this work was to synthesize highly elastic, mechanically stable aerogels that are robust and easy to handle without substantially sacrificing their high porosity or low density. To overcome this challenge, a small amount of readily available and thermally cross-linkable poly(acrylic acid) (PAA) was intermixed with GO to enhance the mechanical integrity of the aerogel without disrupting other desirable characteristic properties. This method is a simple straightforward procedure that does not include multistep or complicated chemical reactions, and it produces aerogels with mass densities of about 4-6 mg cm(-3) and >99.6% porosity that can reversibly support up to 10,000 times their weight with full recovery of their original volume. Finally, pressure sensing capabilities were demonstrated and their oil absorption capacities were measured to be around 120 g oil per g aerogel(-1) which highlights their potential use in practical applications. PMID:25714662

  12. Removal of some basic dyes by poly (Vinyl Alcohol/ acrylic acid)Hydrogel

    A study has made on the preparation and properties of poly (vinyl alcohol/ acrylic acid) hydrogel for the purpose of removal of cationic dyes from aqueous solutions. The effect of dose and monomer concentration on the uptake property of the hydrogel toward dye was studied. The uptake of basic methylene blue-9 dye with PVA/AAc was studied by the batch adsorption technique. The effect of pH on the dye uptake was demonstrated to find out that the suitable pH for maximum uptake occurred at pH 5. It was observed that as the concentration of dye is increased the dye uptake decreased. Furthermore, the uptake of dye by hydrogels increased as the temperature was elevated. The recovery of dye adsorbed is possible by treating the hydrogel with 5% HCl. The results obtained suggested this hydrogel possessed good removal properties towards basic methylene blue-9 dye, and this suggests that such hydrogels could be acceptable for practical uses

  13. Synthesis of poly(acrylic acid) nanogels by preparative pulse radiolysis

    Nanogels are sub-micron size, water-swellable crosslinked structures of hydrophilic polymers. In this work a radiation-based synthesis method that has been previously tested for neutral polymers is applied for production of nanogels of a synthetic polyelectrolyte--poly(acrylic acid) (PAA). In this technique dilute, deoxygenated PAA solution (pH 2) circulating in a closed loop is subjected to pulse irradiation with fast electrons. In each pulse many tens of radicals are instantaneously formed on every macromolecule. One of the major reaction paths of these radicals is intramolecular recombination leading to the formation of nanogels. It is demonstrated that radiation-induced reactions in our system show a typical feature of intramolecular crosslinking, i.e. a strong decrease in dimensions of a polymer coil without an accompanying decrease in molecular weight. In accordance with expectations based on earlier observations on non-polar polymers, intramolecular recombination of PAA-derived radicals proceeds according to non-classical kinetics. A model of non-homogeneous kinetics with time-dependent rate constant has been applied to describe this behaviour and the relationship between kinetic parameters and initial average number of radicals per chain is briefly discussed. The weight-average molecular weight of the products is influenced by side reactions, mainly degradation (chain breakage) and intermolecular crosslinking

  14. Poly(acrylic acid) coating induced 2-line ferrihydrite nanoparticle transport in saturated porous media

    Iron oxide and iron nanoparticles (NPs) have been used effectively for environmental remediation, but are limited in their applications by strong retention in groundwater-saturated porous media. For example, delivery of NPs to large groundwater reservoirs would require large numbers of injection wells. To address this problem, we have explored polymer coatings as a surface engineering strategy to enhance transport of oxide nanoparticles in porous media. We report here on our studies of 2-line ferrihydrite NPs and the influence of poly (acrylic acid) (PAA) polymer coatings on the colloidal stability and transport in natural sand-packed column tests simulating flow in groundwater-saturated porous media. Measurements were also made of zeta potential, hydrodynamic diameter, and polymer adsorption and desorption properties. The coated NPs have a diameter range of 30–500 nm. We found that NP transport was improved by PAA coating and that the transport properties could be tuned by adjusting the polymer concentration. Our results demonstrate that a high stability of oxide particles and improved transport can be achieved in groundwater-saturated porous media by introducing negatively charged polyelectrolytes and optimizing polymer concentrations

  15. Development of Graft Copolymer Flocculant Based on Acrylamide and Acrylic Acid for the dewatering of coal

    Most coal preparation processes were carried out in water medium. The water content of coal product has a negative impact on handling and specific energy value. The moisture content may be attributed to the proportion of fine coal, which presents the greatest dewatering problem. A novel polymeric flocculant has been developed by graft copolymerization of acrylamide (AAm) with acrylic acid (AAc) using gamma irradiation technique. The grafted copol621621ymer P(AAm/AAc) was characterized by Fourier-transform infrared spectroscopy (FTIR), and thermo-gravimetric analysis (TGA). The effects of reaction parameters, such as total absorbed dose, and monomer concentration on grafting yield were investigated. The flocculation performance of the graft copolymer P(AAm/AAc) was investigated in coal suspension. It was observed that the grafting ratio was one of the key factors for the flocculating effects. The copolymers with various grafting ratios showed different flocculating properties. It was found that as the grafting ratio increased, the flocculating effect also increased. The flocculation performance of the grafted copolymer was better than that of the commercial flocculant, poly-acrylamide (Magnafloc 1011).

  16. Poly(acrylic acid) coating induced 2-line ferrihydrite nanoparticle transport in saturated porous media

    Xiang, Aishuang [Princeton University, Chemical and Biological Engineering Department (United States); Yan, Weile [Texas Tech University, Civil and Environmental Engineering (United States); Koel, Bruce E., E-mail: bkoel@princeton.edu [Princeton University, Chemical and Biological Engineering Department (United States); Jaffe, Peter R., E-mail: jaffe@princeton.edu [Princeton University, Civil and Environmental Engineering Department (United States)

    2013-07-15

    Iron oxide and iron nanoparticles (NPs) have been used effectively for environmental remediation, but are limited in their applications by strong retention in groundwater-saturated porous media. For example, delivery of NPs to large groundwater reservoirs would require large numbers of injection wells. To address this problem, we have explored polymer coatings as a surface engineering strategy to enhance transport of oxide nanoparticles in porous media. We report here on our studies of 2-line ferrihydrite NPs and the influence of poly (acrylic acid) (PAA) polymer coatings on the colloidal stability and transport in natural sand-packed column tests simulating flow in groundwater-saturated porous media. Measurements were also made of zeta potential, hydrodynamic diameter, and polymer adsorption and desorption properties. The coated NPs have a diameter range of 30-500 nm. We found that NP transport was improved by PAA coating and that the transport properties could be tuned by adjusting the polymer concentration. Our results demonstrate that a high stability of oxide particles and improved transport can be achieved in groundwater-saturated porous media by introducing negatively charged polyelectrolytes and optimizing polymer concentrations.

  17. Carboxymethyl starch cross-linked by electron beam radiation in presence of acrylic acid sensitizer

    Carboxymethyl starch (CMS) can be cross-linked by electron beam radiation to form a biocompatible and environment-friendly hydrogel at a high absorbed dose and a condensed CMS concentration. Acrylic acid (AAc) can be used as a sensitizer in order to reduce the absorbed doses to an acceptable certain level. At an absorbed dose of 3-4 kGy, the gel content of crosslinked CMS can be obtained about 50% with 5% (w/w) AAc concentration used. The compressive strength of CMS samples increased with increasing their cross-linked densities due to raising absorbed doses. The swelling ratio of cross-linked CMS was also attainable at a maximum of 50 times in the distilled water. The enzymatic degradation of cross-linked CMS was carried out in acetate buffer pH 4.6 with 0.1% α-amylase enzymatic solution incubated at 40℃ for 6 h. The crosslinked CMS samples were degraded slower than uncrosslinked CMS ones. The results indicated that the highly cross-linked CMS was almost fully degradable when the enzymatic hydrolysis was performed during 6 h. The FT IR spectra of cross-linked CMS in the presence of AAc were examined to observe the carboxyl group of AAc in the structure of cross-linked CMS. The hydrophilic of cross-linked CMS surface was determined by a contact-angle analysis. (authors)

  18. Cellulose nanocrystal-filled poly(acrylic acid) nanocomposite fibrous membranes

    Lu, Ping; Hsieh, You-Lo

    2009-10-01

    Nanocomposite fibrous membranes have been fabricated by electrospinning cellulose nanocrystal (CNC)-loaded poly(acrylic acid) (PAA) ethanol mixtures. Incorporating CNC in PAA significantly reduced fiber diameters and improved fiber uniformity. The average diameters of the as-spun nanocomposite fibers were significantly reduced from 349 nm to 162 nm, 141 nm, 90 nm and 69 nm at 5%, 10%, 15% and 20% CNC loading (by weight of a constant 4% PAA solution), respectively. CNC was well dispersed in the fibers as isolated rods oriented along the fiber axis and as spheres in the PAA matrix. The Young modulus and stress of the PAA/CNC nanocomposite fibers were significantly improved with increasing CNC loadings by up to 35-fold and 16-fold, respectively. Heat-induced esterification between the CNC surface hydroxyls and PAA carboxyl groups produced covalent crosslinks at the CNC-PAA interfaces, rendering the nanocomposite fibrous membranes insoluble in water, more thermally stable and far more superior in tensile strength. With 20% CNC, the crosslinked nanocomposite fibrous membrane exhibited a very impressive 77-fold increase in modulus and 58-fold increase in stress.

  19. Cellulose nanocrystal-filled poly(acrylic acid) nanocomposite fibrous membranes

    Nanocomposite fibrous membranes have been fabricated by electrospinning cellulose nanocrystal (CNC)-loaded poly(acrylic acid) (PAA) ethanol mixtures. Incorporating CNC in PAA significantly reduced fiber diameters and improved fiber uniformity. The average diameters of the as-spun nanocomposite fibers were significantly reduced from 349 nm to 162 nm, 141 nm, 90 nm and 69 nm at 5%, 10%, 15% and 20% CNC loading (by weight of a constant 4% PAA solution), respectively. CNC was well dispersed in the fibers as isolated rods oriented along the fiber axis and as spheres in the PAA matrix. The Young modulus and stress of the PAA/CNC nanocomposite fibers were significantly improved with increasing CNC loadings by up to 35-fold and 16-fold, respectively. Heat-induced esterification between the CNC surface hydroxyls and PAA carboxyl groups produced covalent crosslinks at the CNC-PAA interfaces, rendering the nanocomposite fibrous membranes insoluble in water, more thermally stable and far more superior in tensile strength. With 20% CNC, the crosslinked nanocomposite fibrous membrane exhibited a very impressive 77-fold increase in modulus and 58-fold increase in stress.

  20. Removal of cationic dyes by poly(acrylamide-co-acrylic acid) hydrogels in aqueous solutions

    Poly(acrylamide-co-acrylic acid (poly(AAm-co-AAc)) hydrogels prepared by irradiating with γ-radiation were used in experiments on swelling, diffusion, and uptake of some cationic dyes such as Safranine-O (SO) and Magenta (M). Poly(AAm-co-AAc) hydrogels irradiated at 8.0 kGy have been used for swelling and diffusion studies in water and cationic dye solutions. The maximum swellings in water, and SO, and M solutions observed are 2700%, 3500%, and 4000%, respectively. Diffusions of water and cationic dyes within hydrogels have been found to be non-Fickian in character. Adsorption of the cationic dyes onto poly(AAm-co-AAc) hydrogels is studied by the batch adsorption technique. The adsorption type was found Langmuir type in the Giles classification system. The moles of adsorbed dye for SO and M per repeating unit in hydrogel (binding ratio, r) have been calculated as 3834x10-6 and 1323x10-6, respectively. These results show that poly(AAm-co-AAc) hydrogels can be used as adsorbent for water pollutants such as cationic dyes

  1. Syntheses and Crystal Structures of Two Complexes with 3-(3-Pyridyl)acrylic Acid

    2005-01-01

    The reaction of 3-(3-pyridyl)acrylic acid (H(3-PYA)) with Co(NO3)2·6H2O or Complex 1 crystallizes in monoclinic, space group C2/c with a = 9.9473(12), b = 13.7227(16), c =14.7376(18) (A), β = 99.043(2)°, V = 1986.7(4) (A)3, Z = 4, Dc = 1.549 g/cm3, μ = 0.921 mm 1, F(000)= 964, R = 0.0786 and wR = 0.1443. Six types of hydrogen bonds and π-π packing interactions molecular architecture. Complex 2 crystallizes in monoclinic, space group P21/n with a =11.3630(16), b = 7.0346(10), c = 12.1365(18) (A), β = 112.545(3)°, V = 896.0(2) (A)3, Z = 2, Dc =1.997 g/cm3,μ = 0.785 mm-1, F(000) = 438, R = 0.0787 and wR = 0.1550. The discrete entity Mn(Ⅱ)(3-PYD)2(H2O)4 is extended into a 3-D supramolecular architecture by four kinds of hydrogen bonds.

  2. Antimicrobial activity of poly(vinyl alcohol)-poly(acrylic acid) electrospun nanofibers.

    Santiago-Morales, Javier; Amariei, Georgiana; Letón, Pedro; Rosal, Roberto

    2016-10-01

    Electrospun nanofibers were prepared from blends of poly(acrylic acid) (PAA) and poly(vinyl alcohol) (PVA). The fibers were stabilized by heat curing at 140°C via anhydride and ketone formation and crosslinking esterification. The antimicrobial effect was assessed using strains of Escherichia coli and Staphylococcus aureus by tracking their capacity to form colonies and their metabolic impairment upon contact with PAA/PVA membranes. Membranes containing >35wt.% PAA displayed significant antibacterial activity, which was particularly high for the gram-positive S. aureus. All membranes were negatively charged, with surface ζ-potential in the (-34.5)-(-45.6)mV range, but the electrostatic interaction with the negatively charged cells was not the reason for the antimicrobial effect. Neither pH reduction nor the passing of non-crosslinked polymers to the solution affected microbial growth. The antibacterial activity was attributed to the chelation of the divalent cations stabilizing the outer cell membrane. The effect on gram-positive bacteria was attributed to the destabilization of the peptidoglycan layer. The sequestration of divalent cations was demonstrated with experiments in which calcium and a chelating agent were added to the cultures in contact with membranes. The damage to bacterial cells was tracked by measuring their surface charge and the evolution of intracellular calcium during the early stages after contact with PAA/PVA membranes. PMID:27318959

  3. AFM Analysis of Copolymer From Konjac With Acrylic Acid by γ Irradiation

    The water absorption property and atomic force microscopy (AFM) analysis were studied to discover the relativity of water absorption and construction of original konjac powder, grafted copolymer and regenerator. The results show that the water absorption, speed and reserving percent of the grafted copolymer are affected by the size, the liquid ion concentration, the ambient temperature and water reserving time of the gel. At room temperature, the largest water absorption, water absorption speed and water reserving percent of grafted copolymer are 887 times, 64.7 g·g-1·min-1 and 92% in distilled water and 273 times, 27.6 g·g-1·min-1 and 84% in tap water respectively. The AFM images of grafted copolymer indicate that konjac grafts acrylic acid and then hydrophilic structure comes into being. During the course of regeneration the three dimensional structure of the copolymer was changed to more regularly. So the water absorption of copolymer is higher than that of konjac, and the water absorption of regenerator is 360 times, higher than that of copolymer. (authors)

  4. Synthesis and characterization of acrylamide-acrylic acid hydrogels and adsorption of some textile dyes

    Acrylamide (AAm)-acrylic acid (AAc) hydrogels have been prepared at AAm initial compositions of 15%, 20% and 30%. AAm-AAc monomer mixtures have been irradiated in a 60Co-γ source at different doses and percent conversions have been determined gravimetrically. 100% conversion of monomers into hydrogels was achieved at 8 kGy dose. These hydrogels were swollen in distilled water at pH 3.03, 4.18, 4.68, 5.05, 5.30, 6.0, 7.0, 8.0. The results of swelling tests at pH 8.0 indicated that poly(AAm-AAc) hydrogels prepared from solution containing 15% (mol%) AAm showed maximum % swelling as 3000%. Poly(AAm-AAc) hydrogels have been considered for the removal of some textile dyes from aqueous solutions. Among the two common textile dyes tested, Janus Green B (JGB) has showed the highest adsorption capacity while Congo Red (CR) was not adsorbed by these hydrogels. Adsorption isotherms were constructed for JGB and poly(AAm/AAc) gel systems. It is concluded that cross-linked poly(AAm/AAc) hydrogels can be successfully used in the purification of waste water containing certain textile dyes

  5. Preparation and properties of poly(acrylic acid) oligomer stabilized superparamagnetic ferrofluid.

    Lin, Chia-Lung; Lee, Chia-Fen; Chiu, Wen-Yen

    2005-11-15

    Ferrofluids, which are stable dispersions of magnetic particles, behave as liquids that have strong magnetic properties. Nanoparticles of magnetite with a mean diameter of 10-15 nm, which are in the range of superparamagnetism, are usually prepared by the traditional method of co-precipitation from ferrous and ferric electrolyte solution. When diluted, the ferrofluid dispersions are not stable if anionic or cationic surfactants are used as the stabilizer. This work presents an efficient way to prepare a stable aqueous nanomagnetite dispersion. A stable ferrofluid containing Fe3O4 nanoparticles was synthesized via co-precipitation in the presence of poly(acrylic acid) oligomer. The mechanism, microstructure, and properties of the ferrofluid were investigated. The results indicate that the PAA oligomers promoted the nucleation and inhibited the growth of the magnetic iron oxide, and the average diameter of each individual Fe3O4 particle was smaller than 10 nm. In addition, the PAA oligomers provided both electrostatic and steric repulsion against particle aggregation, and the stability of dispersions could be controlled by adjusting the pH value of solution. A small amount of Fe2O3 was found in the nanoparticles but the superparamagnetic behavior of the nanoparticles was not affected. PMID:16009367

  6. Potassium fulvate as co-interpenetrating agent during graft polymerization of acrylic acid from cellulose.

    Ghazy, Mohamed B M; El-Hai, Farag Abd; Mohamed, Magdy F; Essawy, Hisham A

    2016-10-01

    Grafting polymerization of acrylic acid onto cellulose in presence of potassium fulvate (KF) as a co-interpenetrating agent results enhanced water sorption compared to materials prepared similarly in its absence. The insertion of potassium fulvate (KF) did not affect the grafting process and is thought to proceed in parallel to the graft polymerization via intensive polycondensation reactions of its function groups (-COOH and OH) with COOH of the monomer and OH groups of cellulose. The combination of graft copolymerization and polycondensation reactions is assumed to produce interpenetrating network structure. Fourier transform infrared (FTIR) confirmed successful incorporation within the network structure which is an evidence for formation of interpenetrating network. The obtained structures showed homogeneous uniform surface as revealed by scanning electron microscopy (SEM). The obtained superabsorbent possessed high water absorbency 422 and 48.8g/g in distilled water and saline (0.9wt.% NaCl solution), respectively, and enhanced water retention even at elevated temperatures as revealed by thermogravimetric analysis (TGA). This could be explained by the high content of hydrophilic groups. The new superabsorbents proved to be efficient devices for controlled release of fertilizers which expands their use in agricultural applications. PMID:27370745

  7. Synthesis and characterization of zinc chloride containing poly(acrylic acid) hydrogel by gamma irradiation

    In this study, the characterization of zinc chloride incorporated into a poly(acrylic acid) (PAAc) hydrogel prepared by gamma-ray irradiation was investigated. Zinc chloride powder with different concentrations was dissolved in the PAAc solution, and it was crosslinked with gamma-ray irradiation. The effects of various parameters such as zinc ion concentration and irradiation doses on characteristics of the hydrogel formed were investigated in detail for obtaining an antibacterial wound dressing. In addition, the gel content, pH-sensitive (pH 4 or 7) swelling ratio, and UV–vis absorption spectra of the zinc particles in the hydrogels were characterized. Moreover, antibacterial properties of these new materials against Staphylococcus aureus and Escherichia coli strains were observed on solid growth media. The antibacterial tests indicated that the zinc chloride containing PAAc hydrogels have good antibacterial activity. - Highlights: • The characterization of zinc chloride containing PAA hydrogel was investigated. • The gel content increased with an increase in absorbed dose up to 75 kGy. • Finally, the zinc chloride based hydrogels have an antibacterial activity

  8. Poly(acrylic acid) brushes pattern as a 3D functional biosensor surface for microchips

    Wang, Yan-Mei; Cui, Yi; Cheng, Zhi-Qiang; Song, Lu-Sheng; Wang, Zhi-You; Han, Bao-Hang; Zhu, Jin-Song

    2013-02-01

    Poly(acrylic acid) (PAA) brushes, a novel three dimensional (3D) precursor layer of biosensor or protein microarrays, possess high protein loading level and low non-specific protein adsorption. In this article, we describe a simple and convenient way to fabricate 3D PAA brushes pattern by microcontact printing (μCP) and characterize it with FT-IR and optical microscopy. The carboxyl groups of PAA brushes can be applied to covalently immobilize protein for immunoassay. Thriving 3D space made by patterning PAA brushes thin film is available to enhance protein immobilization, which is confirmed by measuring model protein interaction between human immunoglobulin G (H-IgG) and goat anti-H-IgG (G-H-IgG) with fluorescence microscopy and surface plasmon resonance imaging (SPRi). As expected, the SPRi signals of H-IgG coating on 3D PAA brushes pattern and further measuring specific binding with G-H-IgG are all larger than that of 3D PAA brushes without pattern and 2D bare gold surface. We further revealed that this surface can be used for high-throughput screening and clinical diagnosis by label-free assaying of Hepatitis-B-Virus surface antibody (HBsAb) with Hepatitis-B-Virus surface antigen (HBsAg) concentration array chip. The linearity range for HBsAb assay is wider than that of conventional ELISA method.

  9. Graft copolymerization of N-maleoyl-N-phthaloyl-chitosan (MAPHCS) and acrylic acid via γ-ray irradiation

    Chitosan is a well-known abundant natural polymer with good biodegradability, biocompatibility and bioactivity. But its insolubility in common organic solvents of chitosan have hindered its utilization and basic research. N-maleoyl-N-phthaloyl-chitosan (MAPHCS), soluble in DMF or DMSO, was synthesized and characterized by Fourier transform infrared spectra analysis (FT-IR) and 1H-NMR. The graft copolymerization of acrylic acid onto chitosan was carried out with N-maleoyl-N-phthaloyl-chitosan as intermediate in homogeneous system and initiated by γ-irradiation. The double bond of MAPHCS may be the grafting site because the grafting field was much higher than that of the graft copolymerization of acrylic acid and phthaloylchitosan via γ-ray irradiation. The chemical structure of the graft copolymer was characterized by FT-IR and 1H-NMR. As indicated in FTIR spectra, the evidence of the stronger absorbance at 2800-3000 cm-1 for C-H and at 1720 cm-1 for carboxyl group implied significantly the successful introduction of the poly (acrylic acid) on the chitosan chain. Differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA) were also used to characterize the copolymer. Effects of synthesis variables on the graft copolymerization were studied in light of the grafting percentage. The grafting percentage increased with the dose at lower doses, and then decreased. The maximum grafting percentage was up to 132%. (authors)

  10. Radiation grafting of acrylic acid onto partially deacetylated chitin for metal ion adsorbent

    Radiation processing technology is proved to be a useful tool for modification of polymer material including grafting of monomer onto polymer. In this study, partially deacetylated chitin (PD-chitin) was prepared by soaking chitin in NaOH solution with various concentrations from 10% to 50% (w/w) at room temperature for four days. The degree of deacetylation (DD%) of chitin samples was measured by IR spectroscopy method. Radiation grafting of acrylic acid (AAc) onto PD-chitin was carried out by immerging PD-chitin in AAc solution (5-20%v/v) for swelling two days. The swelled PD-chitin sample was filtered and irradiated with Co-60 radiation at dose of 4.8 kGy for grafting. The resulting product, so called PD-chitin-g-PAA was changed to sodium form, PD-chitin-g-PANa by treating with NaOH 1 N and used as metal ion adsorbent. The adsorption capacities of studied chitin samples for metal ion typically for Cu2+ was determined using atomic absorption spectrophotometer. The results showed that the adsorption capacities for Cu2+ were as the following order: chitin L = 15.5 and 19.4 (mg/g); b = 0.02 and 0.04 (L/mg) for PD-chitin and PD-chitin-g-PANa, respectively. The obtained product, PD-chitin-g-PANa can be produced on large scale with competitive cost and used as metal ion adsorbent for water purification as well as for other purposes such as for sorption of dyes and for immobilization of bioactive substances

  11. Radiation grafting of acrylic acid onto partially deacetylated chitin for metal ion adsorbent

    Nguyen Quoc Hien [Research and Development Center for Radiation Technology, Vietnam Atomic Energy Commission, Truong tre Str., Linh xuan, Thu duc, Ho Chi Minh City (Viet Nam)]. E-mail: hiennq@hcm.vnn.vn; Dang Van Phu [Research and Development Center for Radiation Technology, Vietnam Atomic Energy Commission, Truong tre Str., Linh xuan, Thu duc, Ho Chi Minh City (Viet Nam); Nguyen Ngoc Duy [College of Natural Sciences, National University Ho Chi Minh City, 227 Nguyen Van Cu, Ho Chi Minh City (Viet Nam); Ha Thuc Huy [College of Natural Sciences, National University Ho Chi Minh City, 227 Nguyen Van Cu, Ho Chi Minh City (Viet Nam)

    2005-07-01

    Radiation processing technology is proved to be a useful tool for modification of polymer material including grafting of monomer onto polymer. In this study, partially deacetylated chitin (PD-chitin) was prepared by soaking chitin in NaOH solution with various concentrations from 10% to 50% (w/w) at room temperature for four days. The degree of deacetylation (DD%) of chitin samples was measured by IR spectroscopy method. Radiation grafting of acrylic acid (AAc) onto PD-chitin was carried out by immerging PD-chitin in AAc solution (5-20%v/v) for swelling two days. The swelled PD-chitin sample was filtered and irradiated with Co-60 radiation at dose of 4.8 kGy for grafting. The resulting product, so called PD-chitin-g-PAA was changed to sodium form, PD-chitin-g-PANa by treating with NaOH 1 N and used as metal ion adsorbent. The adsorption capacities of studied chitin samples for metal ion typically for Cu{sup 2+} was determined using atomic absorption spectrophotometer. The results showed that the adsorption capacities for Cu{sup 2+} were as the following order: chitin < PD-chitin < PD-chitin-g-PANa < chitosan (DD76%). In addition, equilibrium isotherms were well fitted by Langmuir equation with the constants K {sub L} = 15.5 and 19.4 (mg/g); b = 0.02 and 0.04 (L/mg) for PD-chitin and PD-chitin-g-PANa, respectively. The obtained product, PD-chitin-g-PANa can be produced on large scale with competitive cost and used as metal ion adsorbent for water purification as well as for other purposes such as for sorption of dyes and for immobilization of bioactive substances.

  12. Acetic and Acrylic Acid Molecular Imprinted Model Silicone Hydrogel Materials for Ciprofloxacin-HCl Delivery

    Lyndon Jones

    2012-01-01

    Full Text Available Contact lenses, as an alternative drug delivery vehicle for the eye compared to eye drops, are desirable due to potential advantages in dosing regimen, bioavailability and patient tolerance/compliance. The challenge has been to engineer and develop these materials to sustain drug delivery to the eye for a long period of time. In this study, model silicone hydrogel materials were created using a molecular imprinting strategy to deliver the antibiotic ciprofloxacin. Acetic and acrylic acid were used as the functional monomers, to interact with the ciprofloxacin template to efficiently create recognition cavities within the final polymerized material. Synthesized materials were loaded with 9.06 mM, 0.10 mM and 0.025 mM solutions of ciprofloxacin, and the release of ciprofloxacin into an artificial tear solution was monitored over time. The materials were shown to release for periods varying from 3 to 14 days, dependent on the loading solution, functional monomer concentration and functional monomer:template ratio, with materials with greater monomer:template ratio (8:1 and 16:1 imprinted tending to release for longer periods of time. Materials with a lower monomer:template ratio (4:1 imprinted tended to release comparatively greater amounts of ciprofloxacin into solution, but the release was somewhat shorter. The total amount of drug released from the imprinted materials was sufficient to reach levels relevant to inhibit the growth of common ocular isolates of bacteria. This work is one of the first to demonstrate the feasibility of molecular imprinting in model silicone hydrogel-type materials.

  13. Hydrophobically Modified Polyelectrolytes: V. Interaction of Fluorocarbon Modified Poly (acrylic acid) with Various Added Surfactants

    ZHOU,Hui(周晖); SONG,Guo-Qaiang(宋国强); GUO,Jin-Feng(郭金峰); ZHANG,Yun-xiang (章云祥); DIEING,Reinhold; MA,Lian(马莲); HAEUSSLING,Lukas

    2001-01-01

    The interactions between fiuorocarbon-medified pol(sodium acrylate) and various kinds of added surfactant have been studied by means of viscometric measurement. Association behavior was found in both hydrogenated and fluorinated anionic, nonionic and cationic surfactants. Among them, the interactions between fluorocarbon-modified poly ( sodium acrylate) and cationic surfactants are the strongest, owing to the cooperation of both electrostatic attractions and hydrophobic associations. The anionic surfactants have the weakest effects on the solution properties because of the existence of unfavorable electrostatic repulsion. The hydrophobic interactions between copolymers and fluorinated surfactants are much stronger than those between copolymers and hydrogenated surfactants.

  14. SYNTHESIS AND IN VITRO CHARACTERIZATION OF HYDROXYPROPYL METHYLCELLULOSE-GRAFT-POLY (ACRYLIC ACID/2-ACRYLAMIDO-2-METHYL-1-PROPANESULFONIC ACID) POLYMERIC NETWORK FOR CONTROLLED RELEASE OF CAPTOPRIL.

    Furqan Muhammad, Iqbal; Mahmood, Ahmad; Aysha, Rashid

    2016-01-01

    A super-absorbent hydrogel was developed by crosslinking of 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) and acrylic acid with hydroxypropyl methylcellulose (HPMC) for controlled release drug delivery of captopril, a well known antihypertensive drug. Acrylic acid and AMPS were polymerized and crosslinked with HPMC by free radical polymerization, a widely used chemical crosslinking method. N,N'-methylenebisacrylamide (MBA) and potassium persulfate (KPS) were added as cross-linker and initiator, respectively. The hydrogel formulation was loaded with captopril (as model drug). The concentration of captopril was monitored at 205 nm using UV spectrophotometer. Equilibrium swelling ratio was determined at pH 2, 4.5 and 7.4 to evaluate the pH responsiveness of the formed hydrogel. The super-absorbent hydrogels were evaluated by FTIR, SEM, XRD, and thermal analysis (DSC and TGA). The formation of new copolymeric network was determined by FTIR, XRD, TGA and DSC analysis. The hydrogel formulations with acrylic acid and AMPS ratio of 4: 1 and lower amounts of crosslinker had shown maximum swelling. Moreover, higher release rate of captopril was observed at pH 7.4 than at pH 2, because of more swelling capacity of copolymer with increasing pH of the aqueous medium. The present research work confirms the development of a stable hydrogel comprising of HPMC with acrylic acid and AMPS. The prepared hydrogels exhibited pH sensitive behav-ior. This superabsorbent composite prepared could be a successful drug carrier for treating hypertension. PMID:27008813

  15. SYNTHESIS OF POLY(DIVINYLBENZENE-co-ACRYLIC ACID) HOLLOW MICROSPHERES WITH GOLD NANOPARTICLES ON THE INTERIOR SURFACE

    Wei Liu; Xin-lin Yang; Xu-gang He

    2009-01-01

    Poly(divinylbenzene-co-acrylic acid) (poly(DVB-co-AA)) hollow microspheres with gold nanoparticles on the interior surfaces were prepared from the gold nanoparticles-coated poly(methacrylic acid) (PMAA@Au@poly(DVB-co-AA)) core-shell microspheres by removal of the PMAA core in water.Au nanoparticles-coated PMAA microspheres were afforded by the in-situ reduction of gold trichloride with PMAA microsphere as stabilizer via the interaction between carboxylic acid groups and Au nanoparticles.Gold nanoparticles-coated (PMAA@Au@poly(DVB-co-AA)) microspheres were formed during the distillation precipitation copolymerization of divinylbenzene and acrylic acid in acetonitrile with Au-coated PMAA microspheres as seeds.The thickness of the poly(DVB-co-AA) shell-layer was controlled by the amount of the solvent distilled off the polymerization system.The PMAA microspheres,Au nanoparticles-coated PMAA microspberes,core-shell microspheres,and hollow microspheres with Au nanoparticles on the interior surfaces were studied by transmission electron microscopy and scanning electron microscopy.The stabilization to L-cysteine and the preliminary catalytic property of the Au nanoparticles on the inner surface of hollow poly(DVB-co-AA) microspheres were investigated.

  16. Advances in the Research and Development of Acrylic Acid Production from Biomass%从生物量生产丙烯酸的研究和开发进展

    许晓波; 林建平; 岑沛霖

    2006-01-01

    The shortage of petroleum has resulted in worldwide efforts to produce chemicals from renewable resources. Among these attempts, the possibility of producing acrylic acid from biomass has caught the eye of many researchers. Converting the carbohydrates first to lactic acid by fermentation and then dehydrating lactic acid to acrylic acid is hitherto the most effective way for producing acrylic acid from biomass. While the lactic acid fermentation has been commercialized since longer times, the dehydration process of lactic acid is still under development because of its low yield. Further efforts should be made before this process became economically feasible.Because of the existence of acrylic acid pathways in some microorganisms, strain improvement and metabolic engineering provides also a possibility to produce acrylic acid directly from biomass by fermentation.

  17. Synthesis of hollow silver spheres using poly-(styrene-methyl acrylic acid) as templates in the presence of sodium polyacrylate

    Wang, Aili; Yin, Hengbo; Ge, Chen; Ren, Min; Liu, Yumin; Jiang, Tingshun

    2010-02-01

    Hollow silver spheres were successfully prepared by reducing AgNO 3 with ascorbic acid and using negatively charged poly-(styrene-methyl acrylic acid) (PSA) spheres as templates in the presence of sodium polyacrylate as a stabilizer. Firstly, silver cations adsorbed on the surface of PSA spheres via electrostatic attraction between the carboxyl groups and silver cations were reduced in situ by ascorbic acid. The silver nanoparticles deposited on the surface of PSA spheres served as seeds for the further growth of silver shells. After that, extra amount of AgNO 3 and ascorbic acid solutions were added to form PSA/Ag composites with thick silver shells. In order to obtain compact silver shells, the as-prepared PSA/Ag composites were heated at 150 °C for 3 h. Then hollow silver spheres were prepared by dissolving PSA templates with tetrahydrofuran.

  18. New liner and reticular polyelectrolytes based an acetoacetic ehter and acrylic acid: synthesis, structure and stimulating sensitivity characteristics

    Novel linear and crosslinked poly-carbolytes based on acetoacetic ester and acrylic acid were synthesized for the first time via Michael addition reaction followed by the radical poly-mineralization. The structure and properties of polyelectrolytes were characterized by FTIR, Raman and NMR spectroscopy, TGA, DSC, GPC, viscosimetry, and potentiometric titration. Considerable influence of water content on the swelling rate of hydrogel was established. The swelling-deswelling properties of hydrogels were studied in water-organic solvent mixtures, electric and magnetic fields. (author)

  19. Characterization of interpenetrating networks of acrylic acid (AAc) and N-isopropylacrylamide (NIPAAm) synthesized by ionizing radiation

    Interpenetrating networks of poly(acrylic acid) (PAAc) and poly(N-isopropylacrylamide) (PNIPAAm) were synthesized in two consecutive steps utilizing ionizing radiation in the first step and chemical reaction in the second step. The first network of PAAc hydrogel was formed by ionizing radiation (gamma or electron beam). The secondary gel of PNIPAAm was synthesized directly within the primary gel of PAAc from an aqueous solution of N-isopropylacrylamide (NIPAAm) containing a crosslinking agent, accelerator and redox initiator. The interpenetrating networks (IPNs) were characterized morphologically by scanning electron microscopy (SEM), and their thermal behavior was analyzed by differential scanning calorimetry (DSC) and thermogravimetry analysis (TGA).

  20. IPN's of Acrylic Acid and N-Isopropylacrylamide by Gamma and Electron Beam Irradiation

    In recent years, temperature and pH sensitive hydrogels have been investigated widely because of their unique properties and versatile applications in medicine and biotechnology, as well as drug delivery. However a serious limitation of hydrogels in many applications is the low mechanical strength of such gels when highly swollen. To overcome this problem, sensitive hydrogels were prepared with satisfactory mechanical properties as a semi-interpenetranting network, where one of them is a mechanically stable polymer. In this work temperature sensitive monomer N-isopropylacrylamide (NIPAAm) and a pH sensitive monomer, acrylic acid (AAc) were prepared as an interpenetranting network by a sequential method. Poly (AAc) hydrogels were prepared in glass tubes 3 mm inner diameter, at room temperature from an aqueous solutions 50%vol under argon atmosphere, and irradiated with a Co60 gamma source, at doses from 5 to 30 kGy and dose rate of 3 kGy/h. Poly (AAc) hydrogels were also prepared by electron beam irradiation with a Van de Graaff at a dose rate of 19.4 kGy/min, and radiation doses from 10 to 30 kGy. After polymerization and crosslinking, the gels were washed in water during 48 h, and dried in vacuo to constant weight. Poly (NIPAAm) as secondary gel was synthetized directly within the primary gels in aqueous solution with the croslinker N, N' methylenebisacrylamide (BIS), the accelerator N,N,N,N tetramethyl ethylenediamidne TMEDA, and potasium persulfate as initiator. Equilibrium swelling properties of hydrogels were studied in pH 2.2-8 range and temperature 10-45degree; LCST and pH critic point of the IPN's were determined; the composition of the interpenetrating network was measured by elemental analysis, and the morphological structure characterized by SEM. The volume of the cells of PAAC hydrogels decreased with increase in radiation dose, their mechanic hardness increased and they lost elasticity. The interpenetrating networks of samples with PAAc irradiated at

  1. Chemically Cross-Linked Poly(acrylic-co-vinylsulfonic Acid Hydrogel for the Delivery of Isosorbide Mononitrate

    Talib Hussain

    2013-01-01

    Full Text Available We report synthesis, characterization, and drug release attributes of a series of novel pH-sensitive poly(acrylic-co-vinylsulfonic acid hydrogels. These hydrogels were prepared by employing free radical polymerization using ethylene glycol dimethacrylate (EGDMA and benzyl peroxide (BPO as cross-linker and initiator, respectively. Effect of acrylic acid (AA, polyvinylsulfonic acid (PVSA, and EGDMA on prepared hydrogels was investigated. All formulations showed higher swelling at high pHs and vice versa. Formulations containing higher content of AA and EGDMA show reduced swelling, but one with higher content of PVSA showed increased swelling. Hydrogel network was characterized by determining structural parameters and loaded with isosorbide mononitrate. FTIR confirmed absence of drug polymer interaction while DSC and TGA demonstrated molecular dispersion of drug in a thermally stable polymeric network. All the hydrogel formulations exhibited a pH dependent release of isosorbide mononitrate which was found to be directly proportional to pH of the medium and PVSA content and inversely proportional to the AA contents. Drug release data were fitted to various kinetics models. Results indicated that release of isosorbide mononitrate from poly(AA-co-VSA hydrogels was non-Fickian and that the mechanism was diffusion-controlled.

  2. Gamma radiation synthesis of comb-type graft hydrogels based on poly(acrylic acid) and 4-vinylpyridine

    A pH-sensitive comb-type hydrogel was obtained by gamma radiation polymerization and crosslinking of acrylic acid (AAc) in solution. The pH-sensitive 4-vinylpyridine (4VP) was then grafted to the poly acrylic acid (PAAc) hydrogel using gamma radiation from a 60Co source. The comb type graft polymers obtained (net-PAAc)-g-4VP has been studied through determination of graft yield and swelling behavior. The critical pH value was found to be 5.6. The apparent mechanical properties appear to be qualitatively better than hydrogels of PAAc upon swelling. The new comb-type system presents faster swelling response (30 h) than the polyacrylic acid hydrogel (50 h). The increase in dose rate from 7.3 to 11.3 kGy h-1, increase the radiation grafting percentage of 4VP in the system. Comb-type polymers were also characterized by DSC, TGA and FTIR-ATR. (author)

  3. Effect of acid additives on graft copolymerization and water absorption of graft copolymers of cassava starch and acrylamide/acrylic acid

    Gelatinized cassava starch was radiation graft copolymerized with acrylamide or acrylic acid in the presence of sulfuric acid, nitric acid or maleic acid at a specific dose rate to a fixed total dose. Homopolymer or free copolymer was extracted by water to obtain the pure graft copolymer, which was subsequently saponified with 5% potassium hydroxide solution at room temperature for 90 min. The saponified graft copolymer was investigated for the effect of acid additives and water absorption. The addition of 2% maleic acid into the grafting reaction containing acrylamide-to-starch ratio of 2.5:1 can produce the superabsorbent copolymer having water absorption as high as 2,256 ± 25 g g-1. The effect of acid additive was explained. (author)

  4. Preparation, characterization, and antibacterial activity studies of silver-loaded poly(styrene-co-acrylic acid) nanocomposites

    Song, Cunfeng [Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005 (China); Chang, Ying; Cheng, Ling; Xu, Yiting [Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Chen, Xiaoling, E-mail: tinachen0628@163.com [Department of Endodontics, Xiamen Stomatology Hospital, Teaching Hospital of Fujian Medical University, Xiamen 361003 (China); Zhang, Long; Zhong, Lina [Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China); Dai, Lizong, E-mail: lzdai@xmu.edu.cn [Department of Materials Science and Engineering, College of Materials, Xiamen University, Xiamen 361005 (China)

    2014-03-01

    A simple method for preparing a new type of stable antibacterial agent was presented. Monodisperse poly(styrene-co-acrylic acid) (PSA) nanospheres, serving as matrices, were synthesized via soap-free emulsion polymerization. Field-emission scanning electron microscopy micrographs indicated that PSA nanospheres have interesting surface microstructures and well-controlled particle size distributions. Silver-loaded poly(styrene-co-acrylic acid) (PSA/Ag-NPs) nanocomposites were prepared in situ through interfacial reduction of silver nitrate with sodium borohydride, and further characterized by transmission electron microscopy and X-ray diffraction. Their effects on antibacterial activity including inhibition zone, minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and bactericidal kinetics were evaluated. In the tests, PSA/Ag-NPs nanocomposites showed excellent antibacterial activity against both gram-positive Staphylococcus aureus and gram-negative Escherichia coli. These nanocomposites are considered to have potential application in antibacterial coatings on biomedical devices to reduce nosocomial infection rates. - Highlights: • A new type of antibacterial agent (PSA/Ag-NPs nanocomposites) was synthesized. • The antibacterial activity against S. aureus and E. coli was studied. • Inhibition zone, MIC, MBC, and bactericidal kinetics were evaluated. • PSA/Ag-NPs nanocomposites showed excellent antibacterial activity.

  5. Controlled release of diclofenac sodium from pH-responsive carrageenan-g-poly(acrylic acid) superabsorbent hydrogel

    Hossein Hosseinzadeh

    2010-07-01

    In this paper, controlled release of diclofenac sodium (DS) from pH-sensitive carrageenan-gpoly(acrylic acid) superabsorbent hydrogels was investigated. The hydrogels were prepared by graft copolymerization of acrylic acid (AA) onto kappa-carrageenan, using ammonium persulfate (APS) as a free radical initiator in the presence of methylene bisacrylamide (MBA) as a crosslinker. Infrared spectroscopy was carried out to confirm the chemical structure of the hydrogel. Moreover, morphology of the samples was examined by scanning electron microscopy (SEM). The synthesized hydrogels were subjected to equilibrium swelling studies in simulated gastric and intestinal fluids (SGF and SIF). Hydrogels containing drug DS, at different drug-to-polymer ratios, were prepared by direct adsorption method. The loading yield was found to depend on both the impregnation time and the amount of encapsulated drug. In vitro drug-release studies in different buffer solutions showed that the most important parameter affecting the drug-release behaviour of hydrogels is the pH of the solution. The mechanism involved in release was Fickian ( ≤ 0.43, = 0.348) and Super Case II kinetics ( > 1, = 1.231) at pH 1.2 and 7.4, respectively.

  6. Ultraviolet-induced surface modification of polyurethane films in the presence of oxygen or acrylic acid vapours

    Weibel, Daniel Eduardo, E-mail: danielw@iq.ufrgs.b [Departamento de Fisico-Quimica, Instituto de Quimica, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS (Brazil); Fassini Michels, Alexandre [Centro de Ciencias Exatas e Tecnologia, Universidade de Caxias do Sul, Caxias do Sul, RS (Brazil); Horowitz, Flavio [Laser and Film Optics Laboratory, Instituto de Fisica, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS (Brazil); Silva Cavalheiro, Ricardo da [Departamento de Fisico-Quimica, Instituto de Quimica, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS (Brazil); Vingre da Silva Mota, Gunar [Curso de Fisica, Universidade Federal do Amapa, Macapa, AP (Brazil)

    2009-07-31

    An efficient surface functionalization of polyurethane (PU) films has been obtained by ultraviolet (UV)-assisted modification in the presence of oxygen or acrylic acid (AA) vapours. Film analyses were carried out by water contact angle measurements, X-ray photoelectron spectroscopy (XPS) and Near-edge X-ray absorption fine structure (NEXAFS). Film hydrophilicity increased with photolysis time in the presence of oxygen or AA vapours. Incorporation of COO and C=O functional groups at the polymer surface after the UV-assisted treatments was observed. In addition, High resolution XPS and NEXAFS results showed that a thin film of poly (acrylic acid) (PAA) is formed over the PU films during the UV irradiation with AA vapours. The obtained results are compared with previous published oxygen and AA low-power plasma treatments. Similarity between both treatment methodologies is shown. UV surface functionalization and polymerization of PAA can be used instead of a traditional plasma treatment with the advantage of set-up simplicity and lower costs.

  7. Ultraviolet-induced surface modification of polyurethane films in the presence of oxygen or acrylic acid vapours

    An efficient surface functionalization of polyurethane (PU) films has been obtained by ultraviolet (UV)-assisted modification in the presence of oxygen or acrylic acid (AA) vapours. Film analyses were carried out by water contact angle measurements, X-ray photoelectron spectroscopy (XPS) and Near-edge X-ray absorption fine structure (NEXAFS). Film hydrophilicity increased with photolysis time in the presence of oxygen or AA vapours. Incorporation of COO and C=O functional groups at the polymer surface after the UV-assisted treatments was observed. In addition, High resolution XPS and NEXAFS results showed that a thin film of poly (acrylic acid) (PAA) is formed over the PU films during the UV irradiation with AA vapours. The obtained results are compared with previous published oxygen and AA low-power plasma treatments. Similarity between both treatment methodologies is shown. UV surface functionalization and polymerization of PAA can be used instead of a traditional plasma treatment with the advantage of set-up simplicity and lower costs.

  8. Preparation of acrylic acid-modified chitin improved by an experimental design and its application in absorbing toxic organic compounds

    Huang, Chao-Ming, E-mail: charming@mail.ksu.edu.tw [Department of Materials Engineering, Kun Shan University, Tainan, Taiwan (China); Chen, Lung-Chuan, E-mail: lcchen@mail.ksu.edu.tw [Department of Materials Engineering, Kun Shan University, Tainan, Taiwan (China); Yang, Hui-Chia, E-mail: yang.junkdna@gmail.com [Department of Environmental Engineering, Kun Shan University, Tainan, Taiwan (China); Li, Min-Hsing, E-mail: a1487561a@yahoo.com.tw [Department of Environmental Engineering, Kun Shan University, Tainan, Taiwan (China); Pan, Ting-Chung, E-mail: tcpan@mail.ksu.edu.tw [Department of Environmental Engineering, Kun Shan University, Tainan, Taiwan (China)

    2012-11-30

    Highlights: Black-Right-Pointing-Pointer Acrylic acid-modified chitin. Black-Right-Pointing-Pointer Experimental design. Black-Right-Pointing-Pointer Graft copolymerization. Black-Right-Pointing-Pointer Adsorption of toxic organic compounds. Black-Right-Pointing-Pointer Very high adsorption capacity. - Abstract: Chitin grafted poly (acrylic acid) (chi-g-PAA) is synthesized and characterized as an adsorbent of toxic organic compounds. Chi-g-PAA copolymers are prepared using of ammonium cerium (IV) nitrate (Ce{sup 4+}) as the initiator. The highest grafting percentage of AA in chitin obtained using the traditional technique is 163.1%. A maximum grafting percentage of 230.6% is obtained using central composite design (CCD). Experimental results are consistent with theoretical calculations. The grafted copolymer is characterized by Fourier transform Infrared spectroscopy and solid state {sup 13}C NMR. A representative chi-g-AA copolymer is hydrolyzed to a type of sodium salt (chi-g-PANa) and used in the adsorption of malachite green (MG), methyl violet (MV), and paraquat (PQ) in aqueous. The monolayer adsorption capacities of these substances are 285.7, 357.1, and 322.6 mg/g-adsorbent, respectively. Thermodynamic calculations show that the adsorption of MG, MV, and PQ are more favored at diluted solutions. The high adsorption capacity of chi-g-PANa for toxic matter indicates its potential in the treatment of wastewater and emergency treatment of PQ-poisoned patients.

  9. Antibacterial Effect of Acrylic Acid-Grafted Cotton, Wool and Polyester Fabrics on the Growth of Staphylococcus Aureus

    The effects of nutrient time (t) and acrylic acid graft yield (GY) on the growth of Staphylococcus aureus bacteria on cotton, wool and polyester fabrics have been studied. The bacterial growth increases with the increase in t after a 6 h-incubation period (IP). For cotton fabrics, the IP increases from 6 h to 12 h as the GY increases to 20%. The initial growth rate (R) is found to decrease with the increase in graft yield. The order (n) and rate constant (k) of the growth process are calculated at 303 K from the logarithmic dependence of R on GY. Both kinetic parameters are dependent on the type of fabric. The growth rate constant k is the lowest for grafted cotton and the highest for grafted polyester fabrics. The inhibiting effect of grafted poly acrylic acid (PAA), on the S. aureus growth rate is attributed to the release of hydrogen ions (H+) from the grafts into the nutrient aqueous solution. The accumulation of H+ ions, which increase with the increase in GY, at the cell wall and their possible diffusion inside the cell cause a perturbing effect that impairs the viability of the cells. This is observed from the increase in the polysaccharide layer around the cell due to increase in GY to 20%. Transmission electron micrographs revealed the existence of considerable changes in the shape of the cells as a result of PAA grafted on the fabrics

  10. Radiation Synthesis of Poly(N-Vinyl Pyrrolidone) Nanogels and Nanoscale Grafting of Poly(Acrylic Acid) from Cellulose

    Ionizing radiation has long been known to be a very useful tool for the preparation of nanogels. Although preparation is straightforward, the control of the sizes of nanogels has been a challenging issue. This report shows the results of our work on using radiation for the synthesis of PVP nanogels in the range of 40-200nm by making use of the principles of solution thermodynamics of aqueous polymer solutions. Nanoscale grafting of responsive polymers however has been of scientific and industrial importance due to fine control of the molecular weight and molecular weight distribution of grafted polymers. The second part of this report deals with the grafting of poly(acrylic acid) onto the surface of cellulose, thus imparting pH response to the substrate. The use of radiation as a constant source of radical generation and Reversible-Addition-Fragmentation-Chain transfer agents for the control of free radical polymerization provided a full control over the molecular weight and distribution of poly(acrylic acid) grafts on cellulose. (author)

  11. Dye-sensitized solar cell with poly(acrylic acid-co-acrylonitrile)-based gel polymer electrolyte

    Highlights: ► A nontoxic, easily synthesized poly(acrylic acid-co-acrylonitrile) showed suitable transmittance for dye-sensitized solar cell. ► A cell with relatively large active area fabricated with this polymer material showed acceptable efficiency. ► The gel polymer matrix affected the charge recombination, I3− diffusion, double layer capacitance, and electron lifetime in the cell. - Abstract: A non-conducting, nontoxic poly(acrylic acid-co-acrylonitrile) (PAA) was prepared and used as a supporting matrix for the electrolyte of dye-sensitized solar cells (DSSCs). DSSCs of active area 0.80 cm × 1.10 cm fabricated with PAA, 0.5 M LiI, 0.05 M I2, 0.5 M 3-tert-butylpyridine, and 0.1 M 1-methyl-3-propylimidazolium iodide in 3-methoxypropionitrile solvent showed an average solar energy conversion efficiency of 1.61% under simulated sunlight illumination of 100 mW cm−2, AM 1.5. The effects of the gel polymer matrix on the electrochemical properties of DSSCs were studied using the electrochemical impedance spectroscopy. Relative to the non-gel reference cells, the results showed a decrease in charge recombination, ionic diffusion, and double layer capacitance and an increase in electron lifetime. These results could play an important role in determining the future direction for the development of high-performance gel polymer electrolytes.

  12. Preparation, characterization, and antibacterial activity studies of silver-loaded poly(styrene-co-acrylic acid) nanocomposites

    A simple method for preparing a new type of stable antibacterial agent was presented. Monodisperse poly(styrene-co-acrylic acid) (PSA) nanospheres, serving as matrices, were synthesized via soap-free emulsion polymerization. Field-emission scanning electron microscopy micrographs indicated that PSA nanospheres have interesting surface microstructures and well-controlled particle size distributions. Silver-loaded poly(styrene-co-acrylic acid) (PSA/Ag-NPs) nanocomposites were prepared in situ through interfacial reduction of silver nitrate with sodium borohydride, and further characterized by transmission electron microscopy and X-ray diffraction. Their effects on antibacterial activity including inhibition zone, minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), and bactericidal kinetics were evaluated. In the tests, PSA/Ag-NPs nanocomposites showed excellent antibacterial activity against both gram-positive Staphylococcus aureus and gram-negative Escherichia coli. These nanocomposites are considered to have potential application in antibacterial coatings on biomedical devices to reduce nosocomial infection rates. - Highlights: • A new type of antibacterial agent (PSA/Ag-NPs nanocomposites) was synthesized. • The antibacterial activity against S. aureus and E. coli was studied. • Inhibition zone, MIC, MBC, and bactericidal kinetics were evaluated. • PSA/Ag-NPs nanocomposites showed excellent antibacterial activity

  13. Poly (acrylic acid sodium) grafted carboxymethyl cellulose as a high performance polymer binder for silicon anode in lithium ion batteries.

    Wei, Liangming; Chen, Changxin; Hou, Zhongyu; Wei, Hao

    2016-01-01

    The design of novel binder systems is required for the high capacity silicon (Si) anodes which usually undergo huge volume change during the charge/discharge cycling. Here, we introduce a poly (acrylic acid sodium)-grafted-carboxymethyl cellulose (NaPAA-g-CMC) copolymer as an excellent binder for Si anode in lithium ion batteries (LIBs). The NaPAA-g-CMC copolymer was prepared via a free radical graft polymerization method by using CMC and acrylic acid as precursors. Unlike the linear, one-dimensional binders, the NaPAA-g-CMC copolymer binder is expected to present multi-point interaction with Si surface, resulting in enhanced binding ability with Si particles as well as with the copper (Cu) current collectors, and building a stable solid electrolyte interface (SEI) layer on the Si surface. The NaPAA-g-CMC based Si anode shows much better cycle stability and higher coulombic efficiency than those made with the well-known linear polymeric binders such as CMC and NaPPA. PMID:26786315

  14. NaY zeolites modified by La~(3+) and Ba~(2+): the effect of synthesis details on surface structure and catalytic performance for lactic acid to acrylic acid

    闫婕; 余定华; 李恒; 孙鹏; 黄和

    2010-01-01

    Modified NaY zeolites have been widely studied and the modification metal element is normally single, while few researches have been conducted on NaY zeolites modified by two kinds of metals. In our study, a series of La3+ and Ba2+ modified NaY zeolites were synthesized through different impregnation procedures. Lactic acid dehydration to acrylic acid was selected as a probe reaction to test the catalytic performance of these zeolites synthesized. The effects of synthesis details on their pore structures an...

  15. Physicochemical properties of poly(lactic acid-co-glycolic acid film modified via blending with poly(butyl acrylate-co-methyl methacrylate

    Guoquan Zhu

    2013-01-01

    Full Text Available A series of poly(lactic acid-co-glycolic acid (PLGA/poly(butyl acrylate-co-methyl methacrylate (P(BA-co-MMA blend films with different P(BA-co-MMA mole contents were prepared by casting the polymer blend solution in chloroform. Surface morphologies of the PLGAP(BA-co-MMA blend films were studied by scanning electron microscopy (SEM. Thermal, mechanical, and chemical properties of PLGAP(BA-co-MMA blend films were investigated by differential scanning calorimeter (DSC, thermogravimetric analysis (TGA, tensile tests, and surface contact angle tests. The introduction of P(BA-co-MMA could modify the properties of PLGA films.

  16. The Chemical and Physical Properties of Poly( ε -caprolactone) Scaffolds Functionalised with Poly(vinyl phosphonic acid-co-acrylic acid)

    Bassi, A. K.; Gough, J. E.; Zakikhani, M.; Downes, S

    2011-01-01

    There is a clinical need for a synthetic alternative to bone graft substitute (BGS) derived from demineralised bone matrix. We report the electrospinning of Poly(ε-caprolactone) (PCL) to form a 3-dimensional scaffold for use as a synthetic BGS. Additionally, we have used Poly(vinyl phosphonic acid-co-acrylic acid) (PVPA) to improve bone formation. Fibres were formed using a 10% w/v PCL/acetone solution. Infrared spectroscopy confirmed that the electrospinning process had no effect on the func...

  17. Preparation and characterization of polyacrylamide-modified kaolinite containing poly [acrylic acid-co-methylene bisacrylamide] nanocomposite hydrogels

    Zaharia, Anamaria; Sarbu, Andrei; Radu, Anita-Laura;

    2015-01-01

    Novel nanocomposite hydrogel structures based on cross-linked poly(acrylic acid) (PAA) and kaolinite (Kaol), modified with different loadings of polyacrylamide (PAAm), were prepared by inverse dispersion polymerization. Ceric ammonium nitrate as an initiator in the presence of nitric acid was used...... to graft PAAm from the Kaol surface. The surface-modified Kaol showed enhanced interactions between the filler and the PAA matrix, through interactions between amino (-NH2) from PAAm and carboxylic groups (-COOH) from PAA. The XRD and TEM measurements confirmed the exfoliated nanocomposites with the...... Kaol filler. The swelling degree (SD) of the swollen hydrogel nanocomposite was increased following the addition of polyacrylamide-modified Kaol particles into the hydrogel structures. Rheological characterization showed that an increase in the storage modulus (G') could be a consequence of a good...

  18. Characterization of pH-sensitive Poly (acrylic acid-co-N-vinyl-2-pyrrolidone) Hydrogels Prepared by Gamma Radiation

    YANG Ming-cheng; HE Su-qin; LIU Wen-tao; SONG Hong-yan; ZHU Cheng-shen

    2007-01-01

    The pH-sensitive copolymer hydrogels were prepared with the monomers of acrylic acid and N-vinyl-2-pyrrolidone based on gamma radiation technique. The morphology of the hydrogels was monitored by using scanning electron microscope. The influence of absorbed dose, monomer compasition and concentration on the swelling ratio (SR) of the hydrogels were investigated in detail. The effect of pH and temperature of the swelling medium on the swelling behavior of the hydrogels were also examined. The results show that the SR of the copolymer hydrogels decreases with the monomer concentration and absorbed dose increasing. The copolymer hydrogels show a better pH-sensitive behavior. In alkaline solution, the SR of the hydrogels is much higher than in acid solution.

  19. Effect of time and temperature exposition in the crystallinity degree of sulfonated poly-(styrene acrylic acid) (PSAA-S)

    Duarte, G.W.; Becker, E.B.; Silva, L.; Naspolini, A.M.; Consenso, E.C.; Paula, M.M.S.; Fiori, M.A., E-mail: glau_bn@hotmail.co [University of Extreme South of Santa Catarina Criciuma, SC (Brazil). Dept. of Materials Engineering; Silveira, F.Z. [Federal University of Santa Catarina (UFSC), Florianopolis, SC (Brazil). Dept. of Chemical Engineering

    2010-07-01

    Polymers with special properties have been increasingly applied in the development of technological devices. For example, polymeric materials with special electric properties, such as sulfonated poly-(styrene-acrylic acid) - PSAA-S, are of great interest for showing different conductivities depending on the environment where they are applied. The special properties of PSAA are obtained only after sulfonation step in acidic media. The present work aimed to evaluate the effect of time and temperature exposition in the crystallinity degree of PSAA-S, through a statistical experimental factorial planning. The samples of PSAA-S were submitted to FT-IR and DRX tests. The results showed that the temperature and the time of exposition are significant factors in the crystallinity degree of PSAA-S, considering that the crystal lattices created during the polymerization are damaged by the action of time and temperature at which the polymer is exposed. (author)

  20. Oral delivery of insulin using pH-sensitive hydrogels based on polyvinyl alcohol grafted with acrylic acid/methacrylic acid by radiation

    The pH-responsive hydrogels were studied as a drug carrier for the protection of insulin from the acidic environment of the stomach before releasing in the small intestine. Hydrogels based on poly(vinyl alcohol) networks grafted with acrylic acid or methacrylic acid were prepared via a two-step process. Poly(vinyl alcohol) hydrogels were prepared by gamma ray irradiation (50 kGy) and then followed by grafting either acrylic acid or methacrylic acid onto this poly(vinyl alcohol) hydrogels with subsequent irradiation (5-20 kGy). These graft hydrogels showed pH-sensitive swelling behavior. These hydrogels were used as carrier for the controlled release of insulin. The in vitro release of insulin was observed for the insulin-loaded hydrogels in a simulated intestinal fluid (pH 6.8) but not in a simulated gastric fluid (pH 1.2). The release behavior of insulin in vivo in a rat model confirmed the effectiveness of the oral delivery of insulin to control the level of glucose

  1. Preparation and drug-loading properties of Fe{sub 3}O{sub 4}/Poly(styrene-co-acrylic acid) magnetic polymer nanocomposites

    Lu, Wensheng [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230039 (China); Coordination Chemistry Institute, School of Chemistry and Chemical Engineering and Life Science, Chaohu University, Chaohu 238000 (China); Shen, Yuhua, E-mail: s_yuhua@163.com [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230039 (China); Xie, Anjian [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230039 (China); Zhang, Weiqiang [School of Chemistry and Chemical Engineering, Anhui University, Hefei 230039 (China); Coordination Chemistry Institute, School of Chemistry and Chemical Engineering and Life Science, Chaohu University, Chaohu 238000 (China)

    2013-11-15

    Fe{sub 3}O{sub 4}/poly(styrene-co-acrylic acid) magnetic polymer nanocomposites were synthesized by the dispersion polymerization method using styrene as hard monomer, acrylic acid as functional monomer, Fe{sub 3}O{sub 4} nanoparticles modified with oleic acid as core, and poly(styrene-co-acrylic acid) as shell. Drug-loading properties of magnetic polymer nanocomposites with curcumin as a model drug were also studied. The results indicated that magnetic polymer nanocomposites with monodisperse were obtained, the particle size distribution was 50–120 nm, and the average size was about 100 nm. The contents of poly(styrene-co-acrylic acid) and Fe{sub 3}O{sub 4} nanoparticles in magnetic polymer nanocomposites were 74% and 24.7%, respectively. The drug-loading capacity and entrapment efficiency were 2.5% and 44.4%, respectively. The saturation magnetization of magnetic polymer nanocomposites at 300 K was 20.2 emu/g without coercivity and remanence. The as-prepared magnetic polymer nanocomposites have not only lots of functional carboxyl groups but also stronger magnetic response, which might have potential applications in drug carrier and targeted drug release.

  2. A new coordination mode of (E)-3-(3-hydroxyl-phenyl)-acrylic acid in copper complex: Crystal structure and magnetic properties

    Jin, Xin; Zhou, Pei; Zheng, Chunying [Key Laboratory of Cluster Science of Ministry of Education, School of Chemistry, Beijing Institute of Technology, Beijing 100081 (China); Li, Hui, E-mail: lihui@bit.edu [Key Laboratory of Cluster Science of Ministry of Education, School of Chemistry, Beijing Institute of Technology, Beijing 100081 (China)

    2015-05-15

    A copper complex ([Cu(py){sub 2}(L){sub 2}]·2CH{sub 3}OH){sub n} (HL=(E)-3-(3-hydroxyl-phenyl)-acrylic acid) (1) with acrylic acid ligand was synthesized and structurally analyzed by IR, elemental analysis, TGA and the single-crystal X-ray diffraction methods. It is the first time to find that phenolic hydroxyl of L coordinates to Cu(II). Complex 1 exhibits 1D chain by a double-bridge of ligands, and the 3D supramolecular framework in complex 1 is constructed by π–π stacking interactions and van der Waals Contacts among the 1D chains. The magnetic properties of complex 1 have been studied. - Graphical abstract: A copper complex based on (E)-3-(3-hydroxyl-phenyl)-acrylic acid in a novel coordinated way was synthesized and a ferromagnetic exchange interactions between neighboring Cu(II) ions has be achieved. - Highlights: • A new copper complex with acrylic acid ligand was synthesized and analyzed. • We find the phenolic hydroxyl of MCA ligand coordinates to metal ion firstly. • A ferromagnetic exchange interactions between Cu(II) ions has been achieved.

  3. Poly(glycidyl methacrylate) microspheres: preparation by poly(acrylic acid)-stabilized dispersion polymerization and effect of some reaction parameters

    Koubková, Jana; Horák, Daniel

    2013-01-01

    Roč. 2, č. 3 (2013), s. 218-225. ISSN 2164-9634 R&D Projects: GA ČR GCP207/12/J013 Institutional support: RVO:61389013 Keywords : glycidyl methacrylate * dispersion polymerization * poly(acrylic acid) Subject RIV: CD - Macromolecular Chemistry

  4. Systematic investigation of the synthesis of core-shell poly(styrene-co-acrylic acid) colloids with varying shell thickness and core diameter

    Hinge, Mogens; Keiding, Kristian

    2006-01-01

    (acrylic acid). Further the TEM images of the colloids supported the core-shell morphology of the produced poly(ST-co-AA) colloids. This shows that the produced poly(ST-co-AA) colloids have a core-shell morphology and that the shell thickness can be increased by increasing the acrylic acid concentration in the...... morphology of the material for an specific application is going on. It is known from SFEP of styrene that the final colloidal size can be controlled by adjusting the ionic strength of the synthesis feed [1] and it is suggested that adding acrylic acid to the synthesis will result in a change in...... determined as a function of time. Results show a shift in polymerization from styrene in the core to acrylic acid at the surface during the synthesis. This gives poly(ST-co-AA) colloids that has a core-shell morphology with a core mainly consisting of poly(styrene) and a shell mainly consisting of poly...

  5. A new coordination mode of (E)-3-(3-hydroxyl-phenyl)-acrylic acid in copper complex: Crystal structure and magnetic properties

    A copper complex ([Cu(py)2(L)2]·2CH3OH)n (HL=(E)-3-(3-hydroxyl-phenyl)-acrylic acid) (1) with acrylic acid ligand was synthesized and structurally analyzed by IR, elemental analysis, TGA and the single-crystal X-ray diffraction methods. It is the first time to find that phenolic hydroxyl of L coordinates to Cu(II). Complex 1 exhibits 1D chain by a double-bridge of ligands, and the 3D supramolecular framework in complex 1 is constructed by π–π stacking interactions and van der Waals Contacts among the 1D chains. The magnetic properties of complex 1 have been studied. - Graphical abstract: A copper complex based on (E)-3-(3-hydroxyl-phenyl)-acrylic acid in a novel coordinated way was synthesized and a ferromagnetic exchange interactions between neighboring Cu(II) ions has be achieved. - Highlights: • A new copper complex with acrylic acid ligand was synthesized and analyzed. • We find the phenolic hydroxyl of MCA ligand coordinates to metal ion firstly. • A ferromagnetic exchange interactions between Cu(II) ions has been achieved

  6. Removal of reactive dyes from textile wastewater by immobilized chitosan upon grafted Jute fibers with acrylic acid by gamma irradiation

    Hassan, Mahmoud S.

    2015-10-01

    Jute fibers were grafted with acrylic acid by gamma irradiation technique. Chitosan was immobilized upon the grafted Jute fibers to be used as an adsorbent for waste reactive dye. The treated Jute fibers were characterized by using of Fourier-transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM) and X-ray diffraction (XRD). The effect of Jute treatment on its thermal stability by using thermogravimetric analysis (TGA) and its mechanical properties were investigated. The adsorption isotherm and the different factors affecting the dye adsorption such as pH and contact time were also studied. It was found that the dye adsorption was enhanced in the low pH range and increased with increasing of the contact time, regardless of temperature change.

  7. Preparation and characterization of ZnS/poly(acrylamide-co-acrylic acid) dendritical nanocomposites by γ-irradiation

    Zinc sulfide poly(acrylamide-co-acrylic acid) [ZnS/P(AM-co-AA)] nanocomposites with a dendritical structure were successfully prepared in one step by γ-irradiation technique in an aqueous system at room temperature and under ambient pressure. The results from X-ray powder diffraction (XRD) analysis and IR spectrum of the final product showed the formation of ZnS nanoparticles and the polymerization of monomers, respectively. The photoluminescence (PL) peak of the as-prepared product centered at 450 nm, which showed an obvious red shift compared with the ZnS bulk material. The presence of copolymer was considered to be the main reason that influenced the shape and photoluminescence property of the composite

  8. Improvement in the behavior of bromelain coupled to pNIPAm polymers containing acrylamide or acrylic acid

    Rubab Mahmood

    2014-08-01

    Full Text Available Bromelain was coupled to N-isopropyl acrylamide (NIPAmpolymers, synthesized using NIPAm and various concentrations of acrylamide (Ac or acrylic acid (AAc. Incorporation of Ac/AAcinto the polymer increased the LCST (lower critical solutiontemperature in a concentration dependent manner but AAc wasmore effective in this regard; the LCST rose to 40°C when 6 percent AAc was used. Incorporation of Ac/AAc increased the coupling of enzyme to the polymer and the η (effectiveness factor of the coupled enzyme, moderately. Various studies indicate that such incorporation of hydrophilic monomers into the polymer does not impair its capacity to couple enzyme or expression of the activity of bound enzyme but seems to actually improve the stability of the enzyme against heat induced inactivation and alkaline pH.

  9. Tensile properties of low density polypropylene (LDPE)/palm kernel shell (PKS) biocomposites: The effect of acrylic acid (AA)

    The surface of palm kernel was modified by acrylic acid (AA). Low density polyethylene (LDPE) was filled by palm kernel shell at various 0, 10, 20, 30 and 40 php. The effect of AA as a coupling agent on LDPE/PKS biocomposites on tensile properties and morphology was investigated. The results show that the increasing of filler content decreased the tensile strength and break elongation but increased the Young's modulus. The presence of AA indicates higher tensile strength and Young's modulus but lower elongation at break compared to untreated LDPE/PKS biocomposites. The scanning electron microscope study show that the better interfacial interaction between palm kernel shell and low density polyethylene with addition of AA.

  10. Thermosensitive membranes by radiation-induced graft polymerization of N-isopropyl acrylamide/acrylic acid on polypropylene nonwoven fabric

    Radiation-induced graft copolymerization of N-isopropylacrylamide (NIPAAm) and acrylic acid (AA) mixture was investigated on polypropylene nonwoven fabric to develop a thermosensitive material. The grafting was carried out using methanol, acetone and butanone as homopolymerization inhibitor in the reaction medium. Butanone was observed to give the maximum grafting. It was observed that the grafting is significantly influenced by the reaction conditions, such as radiation dose, monomer concentration, monomer ratio, solvent composition and reaction temperature. The degree of grafting increased as the AA and NIPAAm concentration in the reaction medium increased. The degree of grafting increased as the AA fraction in the NIPAAm/AA mixture increased. The temperature dependence of the grafting process is very much governed by the thermosensitive nature of the grafted chains right from the stage when initial grafting has taken place.

  11. Radiation synthesis of pH-sensitive hydrogels from β-cyclodextrin-grafted PEG and acrylic acid for drug delivery

    A water-soluble macromonomer (PEG-β-CD) was synthesised by reaction of β-cyclodextrin with poly(ethylene glycol) diglycidyl ether. Then, a novel hydrogel with pH-sensitivity was prepared by irradiating the mixture of acrylic acid and PEG-β-CD with electron beam. Compared with the normal PAAc hydrogel, this novel hydrogel had a higher swelling ratio at pH 3-8. 5-Fluorouracil (5-FU) was chosen as a model drug, and the kinetics of 5-FU releasing behavior was studied. Compared with the PAAc hydrogel, the results showed the release time of 5-FU from the cyclodextrin containing hydrogel was prolonged. It may be ascribed to the formation of inclusion complexes between the drug molecules and cyclodextrin groups.

  12. An interesting grafting reactivity of EB preirradiated polypropylene film[Radiation grafting; Polypropylene; Free radical; peroxide; Acrylic acid; Acrylamide

    Chen Jie E-mail: chenjjd@online.sh.cn; Yang Liming; Chen Liqin; Wu Minhong; Nho, Y.C.; Kaetsua, Isao

    2004-02-01

    An interesting grafting reactivity of electron beam preirradiated polypropylene (PP) film was found by grafting of acrylic acid (AAc) and acrylamide (AAm) repeatedly or intermittently. The preirradiated PP film could be grafted several times intermittently and the free radicals or peroxides on the samples could be determined after several times grafting reaction. The effects of storage time, reaction time and repeated reaction times on the degree of grafting were investigated. The trapped radicals, peroxy-radicals and peroxides on the preirradiated and reacted PP films were determined by using electron spin resonance (ESR) and 1,1-diphenyl-2-picryl hydrazyl (DPPH), respectively. An interpenetrating polymer networks (IPN) with both temperature and pH sensitive properties was obtained by two times grafting of AAm and AAc onto preirradiated PP film.

  13. A study on the swelling behavior of poly(acrylic acid) hydrogels obtained by electron beam crosslinking

    Sheikh, N., E-mail: nasheikh@aeoi.org.i [Radiation Applications Research School, Nuclear Science and Technology Research Institute, P.O. Box 11365-3486, Tehran (Iran, Islamic Republic of); Jalili, L. [Polymer group, Technology and Engineering Department, Yazd University, Yazd (Iran, Islamic Republic of); Anvari, F. [Radiation Applications Research School, Nuclear Science and Technology Research Institute, Yazd (Iran, Islamic Republic of)

    2010-06-15

    Poly(acrylic acid) (PAA) hydrogels were prepared by using electron beam (EB) crosslinking of PAA homopolymer from its aqueous solutions. The swelling behavior of the hydrogels was studied as a function of the concentration of PAA solution, radiation dose, pH of the swelling medium and swelling time. Also the environmental pH effect on the water diffusion mode into hydrogels was investigated. These hydrogels clearly showed pH-sensitive swelling behavior with Fickian type of diffusion in the stomach-like pH medium (pH 1.3) and non-Fickian type in the intestine-like pH medium (pH 6.8).

  14. Surface grafted chitosan gels. Part I. Molecular insight into the formation of chitosan and poly(acrylic acid) multilayers

    Liu, Chao; Thormann, Esben; Claesson, Per M.;

    2014-01-01

    Composite polyelectrolyte multilayers of chitosan and low molecular weight poly(acrylic acid) (PAA) have been assembled by sequential adsorption as a first step toward building a surface anchored chitosan gel. Silane chemistry was used to graft the first chitosan layer to prevent film detachment...... and decomposition. The assembly process is characterized by nonlinear growth behavior, with different adsorption kinetics for chitosan and PAA. In situ analysis of the multilayer by means of surface sensitive total internal reflection Raman (TIRR) spectroscopy, combined with target factor analysis of...... steps. The higher molecular weight chitosan shows a similar behavior, although to a much lower extent. Our data demonstrate that the charged monomeric units of chitosan are mainly compensated by carboxylate ions from PAA. Furthermore, the morphology and mechanical properties of the multilayers were...

  15. Preparation of poly(polyethylene glycol methacrylate-co-acrylic acid) hydrogels by radiation and their physical properties

    The pH-responsive copolymer hydrogels were prepared with the monomers of polyethylene glycol methacrylate and acrylic acid based on γ-ray irradiation technique. The gel content of these copolymer hydrogels varied depending on both the composition of monomers and the radiation dose. Maximum gel percent and degree of crosslinking were obtained at the composition of equal amount of comonomers. These copolymer hydrogels did not show any noticeable change in swelling at lower pH range. However they showed an abrupt increase in swelling at higher pH range due to the ionization of carboxyl groups. This pH-responsive swelling behavior was applied for the insulin carrier via oral delivery. Insulin-loaded copolymer hydrogels released most of their insulin in the simulated intestinal fluid which had a pH of 6.8 but not in the simulated gastric fluid which had a pH of 1.2

  16. PHOTO-INDUCED DOPED POLYANILINE BY THE VINYLIDENE CHLORIDE AND METHYL ACRYLATE COPOLYMER AS PHOTO ACID GENERATOR

    LI Suzhen; WAN Meixiang

    1997-01-01

    The emeraldine base form of polyaniline (PANI) can be doped by a photo-induced doping method. In this method a copolymer of vinylidene chloride and methyl acrylate (VCMAC) was used as photo acid generator which can release proton when it is exposed to ultraviolet light (λ = 254 nm). The structure of PANI-VCMAC system before and after irradiation was characterized by elemental analysis, IR, XPS, and SEM images. Results obtained indicate that the photo-induced doping characteristics, such as doping position and type of charge carriers, are similar to that of PANI doped with HCl. The poor roomtemperature conductivity (~ 10-5S/cm) of PANI-VCMAC system after irradiation may be due to low doping degree (~pH= 3) and the difference in morphology as compared with PANI-HCl film.

  17. Effect of thermal treatment conditions on properties of vanadium molybdenum oxide catalyst in acrolein oxidation reaction to acrylic acid

    The effect of thermal treatment conditions (temperature and gas medium) on properties of vanadium molybdenum oxide catalyst in acrolein oxidation reaction to acrylic acid is investigated. It is shown that active and selective catalysts are formed in the course of thermal decomposition of the drying product of ammonium metavanadate and paramolybdate under the conditions ensuring the vanadium ion reduction up to tetravalent state with conservation of molybdenum oxidation degree equal to 6. It is possible to realize it either by treatment of the catalyst calcinated in the air flow at 300 deg by the reaction mixture at the activation stage or by gas-reducer flow treatment at 280 deg. Thermal treatment in the reducing medium of the oxidized catalyst does not lead to complete regeneration of its properties

  18. SYNTHESIS OF SOAP-FREE ACRYLIC HYDROSOLS

    Li Jia; Zong-hui Liu; De-qing Wei

    2002-01-01

    Poly(methyl methacrylate/ethyl acrylate/acrylic acid) hydrosols were prepared by employing soap-freepolymerization, and (acrylic acid/butyl acrylate) oligomer was used as the polymeric surfactant. The effect of reactioncondition on the morphology and particle size of the hydrosols was investigated. The minimum amount of acrylic acid in thehydrosols is 2%. The maximum weight average molecular weight (Mw) of polymer that assures soap-free emulsionconversion into hydrosol is about 1.2 × 105-1.3 × 105. The particle transforming process was investigated, and an obviouschange of particle diameter and morphology was observed.

  19. Calcium Phosphate Mineralization in Cellulose Derivative/Poly(acrylic acid) Composites Having a Chiral Nematic Mesomorphic Structure.

    Ogiwara, Takuya; Katsumura, Ayaka; Sugimura, Kazuki; Teramoto, Yoshikuni; Nishio, Yoshiyuki

    2015-12-14

    Calcium phosphate mineralization was conducted by using polymer composites of liquid-crystalline (ethyl)cellulose (EC) or (hydroxypropyl)cellulose (HPC) with poly(acrylic acid) (PAA) as a scaffolding medium for the inorganic deposition. The EC/PAA and HPC/PAA samples were prepared in colored film form from EC and HPC lyotropic liquid crystals of left-handed and right-handed chiral nematics, respectively, by polymerization and cross-linking of acrylic acid as the main solvent component. The mineralization was allowed to proceed in a batchwise operation by soaking the liquid-crystalline films in an aqueous salt solution containing the relevant ions, Ca(2+) and HPO4(2-). The calcium phosphate-deposited EC/PAA and HPC/PAA composites (weight gain, typically 15-25% and 6-11%, respectively) retained the chiral nematic organization of the respective original handedness but exhibited selective light-reflection of longer wavelengths relative to that of the corresponding nonmineralized samples. From X-ray diffraction and energy-dispersive X-ray spectroscopy measurements, it was deduced that the calcium and phosphorus were incorporated inside the polymer matrices in three forms: amorphous calcium phosphate, hydroxyapatite, and a certain complex of PAA-Ca(2+). Dynamic mechanical analysis and thermogravimetry revealed that the inorganic hybridization remarkably enhanced the thermal and mechanical performance of the optically functionalized cellulosic/synthetic polymer composites; however, the effect was more drastic in the EC/PAA series rather than the HPC/PAA series, reflecting the difference in the deposited mineral amount between the two. PMID:26536381

  20. Preparation and characterization of mucus-penetrating papain/poly(acrylic acid) nanoparticles for oral drug delivery applications

    Particle diffusion through the intestinal mucosal barrier is restricted by the viscoelastic and adhesive properties of the mucus gel layer, preventing their penetration to the underlying absorptive endothelial cells. To overcome this natural barrier, we developed nanoparticles which have a remarkable ability to cleave mucoglycoprotein substructures responsible for the structural and rheological properties of mucus. After rheological screening of various mucolytic proteases, nanoparticles composed of poly(acrylic acid) and papain were prepared and characterized regarding particle size and zeta potential. Analysis of nanoparticles showed mean diameters sub-200 nm (162.8–198.5 nm) and negative zeta potentials advancing the mobility in mucus gel. Using diffusion chamber studies and the rotating diffusion tubes method, we compared the transport rates of papain modified (PAPC) and unaltered poly(acrylic acid) (PAA) particles through freshly excised intestinal porcine mucus. Results of the diffusion assays demonstrated strongly enhanced permeation behavior of PAPC particles owing to local mucus disruption by papain. Improved transport rates, reduction in mucus viscosity and the retarded release of hydrophilic macromolecular compounds make proteolytic enzyme functionalized nanoparticles of substantial interest for improved targeted drug delivery at mucosal surfaces. Although cytotoxicity tests of the nanoparticles could not be performed, safety of papain and PAA was already verified making PAPC particles a promising candidate in the pharmaceutical field of research. The focus of the present study was the development of particles which penetrate the mucus barrier to approach the underlying epithelium. Improvements of particles that penetrate the mucus followed by cell uptake in this direction are ongoing.

  1. Preparation and characterization of mucus-penetrating papain/poly(acrylic acid) nanoparticles for oral drug delivery applications

    Mueller, Christiane; Leithner, Katharina; Hauptstein, Sabine; Hintzen, Fabian [Center for Molecular Biosciences Innsbruck, University of Innsbruck, CCB-Centrum for Chemistry und Biomedicine, Department of Pharmaceutical Technology, Institute of Pharmacy (Austria); Salvenmoser, Willi [University of Innsbruck, Department for Evolutionary Developmental Biology, Institute of Zoology and Center for Molecular Biosciences (Austria); Bernkop-Schnuerch, Andreas, E-mail: andreas.bernkop@uibk.ac.at [Center for Molecular Biosciences Innsbruck, University of Innsbruck, CCB-Centrum for Chemistry und Biomedicine, Department of Pharmaceutical Technology, Institute of Pharmacy (Austria)

    2013-01-15

    Particle diffusion through the intestinal mucosal barrier is restricted by the viscoelastic and adhesive properties of the mucus gel layer, preventing their penetration to the underlying absorptive endothelial cells. To overcome this natural barrier, we developed nanoparticles which have a remarkable ability to cleave mucoglycoprotein substructures responsible for the structural and rheological properties of mucus. After rheological screening of various mucolytic proteases, nanoparticles composed of poly(acrylic acid) and papain were prepared and characterized regarding particle size and zeta potential. Analysis of nanoparticles showed mean diameters sub-200 nm (162.8-198.5 nm) and negative zeta potentials advancing the mobility in mucus gel. Using diffusion chamber studies and the rotating diffusion tubes method, we compared the transport rates of papain modified (PAPC) and unaltered poly(acrylic acid) (PAA) particles through freshly excised intestinal porcine mucus. Results of the diffusion assays demonstrated strongly enhanced permeation behavior of PAPC particles owing to local mucus disruption by papain. Improved transport rates, reduction in mucus viscosity and the retarded release of hydrophilic macromolecular compounds make proteolytic enzyme functionalized nanoparticles of substantial interest for improved targeted drug delivery at mucosal surfaces. Although cytotoxicity tests of the nanoparticles could not be performed, safety of papain and PAA was already verified making PAPC particles a promising candidate in the pharmaceutical field of research. The focus of the present study was the development of particles which penetrate the mucus barrier to approach the underlying epithelium. Improvements of particles that penetrate the mucus followed by cell uptake in this direction are ongoing.

  2. Poly(vinyl alcohol)/poly(acrylic acid)/TiO2/graphene oxide nanocomposite hydrogels for pH-sensitive photocatalytic degradation of organic pollutants

    Graphical abstract: The photocatalytic removal of pollutants was improved by the two-step mechanism based on the adsorption of pollutants by hydrogel and the effective decomposition by combination of TiO2 and graphene oxide. -- Highlights: • pH sensitive PVA/PAAc hydrogels were prepared by radical polymerization and condensation reaction. • PVA/PAAc/TiO2/graphene oxide nanocomposite hydrogels were used for treatment of basic waste water. • Photocatalytic acitivity of TiO2 was improved by incorporation of graphene oxide. • Photocatalytic decomposition by nanocomposite hydrogel was improved by increasing pH. -- Abstract: Poly(vinyl alcohol)/poly(acrylic acid)/TiO2/graphene oxide nanocomposite hydrogels were prepared using radical polymerization and condensation reaction for the photocatalytic treatment of waste water. Graphene oxide was used as an additive to improve the photocatalytic activity of poly(vinyl alcohol)/poly(acrylic acid)/TiO2 nanocomposite hydrogels. Both TiO2 and graphene oxide were immobilized in poly(vinyl alcohol)/poly(acrylic acid) hydrogel matrix for an easier recovery after the waste water treatment. The photocatalytic activity of poly(vinyl alcohol)/poly(acrylic acid)/TiO2/graphene oxide nanocomposite hydrogels was evaluated on the base of the degradation of pollutants by using UV spectrometer. The improved removal of pollutants was due to the two-step mechanism based on the adsorption of pollutants by nanocomposite hydrogel and the effective decomposition of pollutants by TiO2 and graphene oxide. The highest swelling of nanocomposite hydrogel was observed at pH 10 indicating that poly(vinyl alcohol)/poly(acrylic acid)/TiO2/graphene oxide nanocomposite hydrogels were suitable as a promising system for the treatment of basic waste water

  3. Poly(vinyl alcohol)/poly(acrylic acid)/TiO{sub 2}/graphene oxide nanocomposite hydrogels for pH-sensitive photocatalytic degradation of organic pollutants

    Moon, Young-E; Jung, Gowun; Yun, Jumi; Kim, Hyung-Il, E-mail: hikim@cnu.ac.kr

    2013-10-01

    Graphical abstract: The photocatalytic removal of pollutants was improved by the two-step mechanism based on the adsorption of pollutants by hydrogel and the effective decomposition by combination of TiO{sub 2} and graphene oxide. -- Highlights: • pH sensitive PVA/PAAc hydrogels were prepared by radical polymerization and condensation reaction. • PVA/PAAc/TiO{sub 2}/graphene oxide nanocomposite hydrogels were used for treatment of basic waste water. • Photocatalytic acitivity of TiO{sub 2} was improved by incorporation of graphene oxide. • Photocatalytic decomposition by nanocomposite hydrogel was improved by increasing pH. -- Abstract: Poly(vinyl alcohol)/poly(acrylic acid)/TiO{sub 2}/graphene oxide nanocomposite hydrogels were prepared using radical polymerization and condensation reaction for the photocatalytic treatment of waste water. Graphene oxide was used as an additive to improve the photocatalytic activity of poly(vinyl alcohol)/poly(acrylic acid)/TiO{sub 2} nanocomposite hydrogels. Both TiO{sub 2} and graphene oxide were immobilized in poly(vinyl alcohol)/poly(acrylic acid) hydrogel matrix for an easier recovery after the waste water treatment. The photocatalytic activity of poly(vinyl alcohol)/poly(acrylic acid)/TiO{sub 2}/graphene oxide nanocomposite hydrogels was evaluated on the base of the degradation of pollutants by using UV spectrometer. The improved removal of pollutants was due to the two-step mechanism based on the adsorption of pollutants by nanocomposite hydrogel and the effective decomposition of pollutants by TiO{sub 2} and graphene oxide. The highest swelling of nanocomposite hydrogel was observed at pH 10 indicating that poly(vinyl alcohol)/poly(acrylic acid)/TiO{sub 2}/graphene oxide nanocomposite hydrogels were suitable as a promising system for the treatment of basic waste water.

  4. Structure- Property Behavior of Poly (acrylic acid) Hydrogels Synthesized by Radiation Induced Polymerization

    Hydrogel containing hydroxyl group based on glycerol, ethylene glycol and acrylic monomer, have been prepared by using gamma radiation. The application of the prepared hydrogel for recovery of CU2+, Co2+, Ni2+, and Pb2+ was also studied. The hydrogel for complexes with metals have been isolated and characterized by using different spectroscopic techniques IR and thermal analysis. TGA thermo grams were used to determine the kinetic parameters such as activation energy and order of reaction. The complexometric titration showed that the hydrogels have a great affinity to recover the metal ions in the following order Pb2+ > Ni2+ > Cu2+ > Co2+. However the hydrogel containing glycerol has a great tendency towards metals recovery than than the one containing ethylene glycol

  5. RAFT-Mediated Polymerization-Induced Self-Assembly of Poly(Acrylic Acid-b-Poly(Hexafluorobutyl Acrylate: Effect of the pH on the Synthesis of Self-Stabilized Particles

    Jianhua Zhou

    2016-05-01

    Full Text Available This paper describes a very simple strategy towards self-stabilized poly(acrylic acid-block-poly(hexafluorobutyl acrylate (PAA-b-PHFBA block copolymer particles via reversible addition-fragmentation chain transfer (RAFT-mediated polymerization-induced self-assembly. Hexafluorobutyl acrylate (HFBA monomer conversion and number-average molar mass of PAA-b-PHFBA increased gradually with the increase in the pH value of the aqueous phase. When pH < 10, the molecular weight distributions of PAA-b-PHFBA were narrow, however, when the pH was raised to 11.55, PAA-b-PHFBA block copolymers had a broader distribution (ĐM = 1.82 with a serious trailing toward the low molecular weight. Furthermore, the morphology and size of PAA-b-PHFBA latex particles were measured by transmission electron microscopy and dynamic light scattering. The results indicated that the PAA-b-PHFBA latex particles had a clear spherical core-shell structure and the latex particles’ size increased with the increase of pH value.

  6. In vitro release studies of vitamin B12 from poly N-vinyl pyrrolidone /starch hydrogels grafted with acrylic acid synthesized by gamma radiation

    Co-polymeric hydrogels containing N-vinyl pyrrolidone and starch grafted with acrylic acid were synthesized by gamma radiation. Their gel contents, grafting process and swelling were evaluated. The gels were also characterized by thermal gravimetric analysis. The gel content found to be increase with increasing the irradiation dose up to 50 kGy then decrease. The grafting percent increase by increasing the percentage of acrylic acid in the grafted hydrogels. The thermal stability and the rate of the thermal decomposition showed to be changed according to the different composition of the hydrogels. It also showed a decrease in the maximum rate of the thermal decomposition by the increasing of the irradiation dose from 20 to 30 kGy and increases by increasing the irradiation dose from 30 to 70 kGy. The hydrogels loaded with vitamin B12 as drug model, demonstrated a decrease release in acidic medium than the neutral one

  7. Radiation Synthesis of Stimuli-Responsive Hydrogels and Their Interactions with Poly(acrylic acid) and Ionic Surfactants

    those with high content of hydrophobic moiety. Considerable improvement of thermo-induced collapse behavior, namely high amplitude and narrower temperature interval of collapse was shown for the certain sample. In the present work also novel pH-responsive hydrogels of cationic and amphoteric nature were synthesized by gamma-radiation copolymerization of vinyl ethers of monoethanolamine (VEMEA) and ethyleneglycol (VEEG) as well as VEMEA and acrylic acid (AA). The synthesis regularities have been studied. The effects of the feed mixture, cross-linker concentration, absorbed dose on the gel/sol fractions and swelling behavior of the hydrogels is studied. The swelling behavior of the hydrogels was studied as a function of pH. It was found that the isoelectric point of the polyampholyte hydrogels based on VEMEA and AA depends on the composition of copolymers. The interactions of the amphoteric hydrogels based on VEMEA and AA with linear poly(acrylic acid) and poly(vinyl ether of monoethanolamine) lead to the formation of gel-polymer interpolyelectrolyte compexes. It was demonstrated that the cationic hydrogels VEMEA-VEEG are able to bind poly(acrylic acid) to form polyelectrolyte complexes with swelling properties typical for polyampholytes

  8. Vinyl ether/acrylic acid terpolymer hydrogels synthesized by γ-radiation: characterization, thermosensitivity and pH-sensitivity

    The radiation copolymerization of hydrophilic ethylene glycol vinyl ether (EGVE), hydrophobic butyl vinyl ether (BVE) and/or acidic comonomer acrylic acid (AA) was realized in the presence of crosslinking agent diethylene glycol divinyl ether (DEGDVE). The swelling studies which were carried out at 4 and 37 deg. C in phosphate buffer solution (PBS, pH 7.4) showed that equilibrium swelling ratios of the hydrogels (except EGVE homopolymer hydrogel) decreases with increasing temperature and swelling process obeys non-Fickian diffusion mechanism. The pH-dependent swelling behaviour of the hydrogels was examined in buffered solutions at various pHs. The swelling process is reversible and pH-dependent for the AA-containing hydrogel. While this hydrogel shows a fully hydrated form at pH>6; it extensively dehydrates below pH 6. The gels are stable after the repeated swelling experiments. The molecular structure of the hydrogels was studied by Fourier Transform Infrared Spectroscopy and their thermal behaviour was investigated by Differential Scanning Calorimetry and Thermal Gravimetric Analysis. The surface and cross-section structures of the gels were examined by a Scanning Electron Microscope

  9. Optimal Design for Reactivity Ratio Estimation: A Comparison of Techniques for AMPS/Acrylamide and AMPS/Acrylic Acid Copolymerizations

    Alison J. Scott

    2015-11-01

    Full Text Available Water-soluble polymers of acrylamide (AAm and acrylic acid (AAc have significant potential in enhanced oil recovery, as well as in other specialty applications. To improve the shear strength of the polymer, a third comonomer, 2-acrylamido-2-methylpropane sulfonic acid (AMPS, can be added to the pre-polymerization mixture. Copolymerization kinetics of AAm/AAc are well studied, but little is known about the other comonomer pairs (AMPS/AAm and AMPS/AAc. Hence, reactivity ratios for AMPS/AAm and AMPS/AAc copolymerization must be established first. A key aspect in the estimation of reliable reactivity ratios is design of experiments, which minimizes the number of experiments and provides increased information content (resulting in more precise parameter estimates. However, design of experiments is hardly ever used during copolymerization parameter estimation schemes. In the current work, copolymerization experiments for both AMPS/AAm and AMPS/AAc are designed using two optimal techniques (Tidwell-Mortimer and the error-in-variables-model (EVM. From these optimally designed experiments, accurate reactivity ratio estimates are determined for AMPS/AAm (rAMPS = 0.18, rAAm = 0.85 and AMPS/AAc (rAMPS = 0.19, rAAc = 0.86.

  10. Mechanism of poly(acrylic acid) acceleration of antithrombin inhibition of thrombin: implications for the design of novel heparin mimics.

    Monien, Bernhard H; Cheang, Kai I; Desai, Umesh R

    2005-08-11

    The bridging mechanism of antithrombin inhibition of thrombin is a dominant mechanism contributing a massive approximately 2500-fold acceleration in the reaction rate and is also a key reason for the clinical usage of heparin. Our recent study of the antithrombin-activating properties of a carboxylic acid-based polymer, poly(acrylic acid) (PAA), demonstrated a surprisingly high acceleration in thrombin inhibition (Monien, B. H.; Desai, U. R. J. Med. Chem. 2005, 48, 1269). To better understand this interesting phenomenon, we have studied the mechanism of PAA-dependent acceleration in antithrombin inhibition of thrombin. Competitive binding studies with low-affinity heparin and a heparin tetrasaccharide suggest that PAA binds antithrombin in both the pentasaccharide- and the extended heparin-binding sites, and these results are corroborated by molecular modeling. The salt-dependence of the K(D) of the PAA-antithrombin interaction shows the formation of five ionic interactions. In contrast, the contribution of nonionic forces is miniscule, resulting in an interaction that is significantly weaker than that observed for heparins. A bell-shaped profile of the observed rate constant for antithrombin inhibition of thrombin as a function of PAA concentration was observed, suggesting that inhibition proceeds through the "bridging" mechanism. The knowledge gained in this mechanistic study highlights important rules for the rational design of orally available heparin mimics. PMID:16078853